ClinVar for MedGen (Select 400655) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3024319	NM_001165963.4(SCN1A):c.1285C>A (p.Gln429Lys)	SCN1A (Q429K)	Single nucleotide variant (missense variant +2 more)	Migraine, familial hemiplegic, 3 +3 more	GPathogenic
Select item 3024230	NM_001165963.4(SCN1A):c.241G>A (p.Asp81Asn)	SCN1A (D81N)	Single nucleotide variant (missense variant +2 more)	Migraine, familial hemiplegic, 3 +3 more	GPathogenic
Select item 2500082	NM_001165963.4(SCN1A):c.5263G>A (p.Asp1755Asn)	LOC102724058, SCN1A (D1726N +5 more)	Single nucleotide variant (missense variant +1 more)	Severe myoclonic epilepsy in infancy +3 more	GUncertain significance
Select item 2430163	NM_001165963.4(SCN1A):c.2589+2dup	SCN1A	Duplication (splice donor variant)	Severe myoclonic epilepsy in infancy +3 more	GLikely pathogenic
Select item 1704267	NM_001165963.4(SCN1A):c.828A>C (p.Lys276Asn)	SCN1A (K276N)	Single nucleotide variant (missense variant +2 more)	Migraine, familial hemiplegic, 3	GPathogenic
Select item 1704266	NM_001165963.4(SCN1A):c.4924A>G (p.Arg1642Gly)	LOC102724058, SCN1A (R1613G +5 more)	Single nucleotide variant (missense variant +1 more)	Migraine, familial hemiplegic, 3	GLikely pathogenic
Select item 1704265	NM_001165963.4(SCN1A):c.659T>A (p.Val220Asp)	SCN1A (V220D)	Single nucleotide variant (missense variant +2 more)	Migraine, familial hemiplegic, 3	GPathogenic
Select item 1704264	NM_001165963.4(SCN1A):c.2946+2T>C	SCN1A	Single nucleotide variant (splice donor variant)	Migraine, familial hemiplegic, 3	GPathogenic
Select item 1704263	NM_001165963.4(SCN1A):c.2854T>A (p.Trp952Arg)	SCN1A (W138R +5 more)	Single nucleotide variant (missense variant +1 more)	Migraine, familial hemiplegic, 3	GPathogenic
Select item 1704262	NM_001165963.4(SCN1A):c.2732T>G (p.Leu911Arg)	SCN1A (L882R +5 more)	Single nucleotide variant (missense variant +1 more)	Migraine, familial hemiplegic, 3	GLikely pathogenic
Select item 1679753	NM_001165963.4(SCN1A):c.-142G>A	SCN1A	Single nucleotide variant (splice acceptor variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +3 more	GUncertain significance
Select item 1492924	NM_001165963.4(SCN1A):c.2415+9A>G	SCN1A	Single nucleotide variant (5 prime UTR variant +1 more)	Severe myoclonic epilepsy in infancy +4 more	GLikely benign
Select item 1418113	NM_001165963.4(SCN1A):c.811G>A (p.Gly271Ser)	SCN1A (G271S)	Single nucleotide variant (missense variant +2 more)	Migraine, familial hemiplegic, 3 +4 more	GPathogenic/Likely pathogenic
Select item 1359475	NM_001165963.4(SCN1A):c.1457C>G (p.Ala486Gly)	SCN1A (A485G +1 more)	Single nucleotide variant (missense variant +2 more)	Migraine, familial hemiplegic, 3 +4 more	GConflicting classifications of pathogenicity
Select item 1057080	NM_001165963.4(SCN1A):c.1169T>C (p.Leu390Pro)	SCN1A (L390P)	Single nucleotide variant (missense variant +2 more)	Migraine, familial hemiplegic, 3 +4 more	GPathogenic/Likely pathogenic
Select item 1052445	NM_001165963.4(SCN1A):c.5822C>A (p.Thr1941Lys)	LOC102724058, SCN1A (T1127K +5 more)	Single nucleotide variant (missense variant +1 more)	Early infantile epileptic encephalopathy with suppression bursts	GUncertain significance
Select item 1027787	NM_001165963.4(SCN1A):c.4300T>A (p.Trp1434Arg)	LOC102724058, SCN1A (W1423R +5 more)	Single nucleotide variant (missense variant +1 more)	Migraine, familial hemiplegic, 3 +1 more	GConflicting classifications of pathogenicity
Select item 1007573	NM_001165963.4(SCN1A):c.2477A>G (p.Tyr826Cys)	SCN1A (Y12C +5 more)	Single nucleotide variant (missense variant +1 more)	Migraine, familial hemiplegic, 3 +4 more	GUncertain significance
Select item 960282	NM_001165963.4(SCN1A):c.839G>A (p.Trp280Ter)	SCN1A (W280*)	Single nucleotide variant (nonsense +2 more)	Migraine, familial hemiplegic, 3 +4 more	GPathogenic
Select item 957895	NM_001165963.4(SCN1A):c.3478G>A (p.Gly1160Ser)	LOC102724058, SCN1A (G1148S +5 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +4 more	GConflicting classifications of pathogenicity
Select item 932130	NM_001165963.4(SCN1A):c.1028+2T>C	SCN1A	Single nucleotide variant (splice donor variant)	Early infantile epileptic encephalopathy with suppression bursts +1 more	GPathogenic
Select item 931957	NM_001165963.4(SCN1A):c.4019T>C (p.Leu1340Pro)	LOC102724058, SCN1A (L1328P +5 more)	Single nucleotide variant (missense variant +1 more)	Migraine, familial hemiplegic, 3	GLikely pathogenic
Select item 931824	NM_001165963.4(SCN1A):c.4772A>T (p.Lys1591Ile)	LOC102724058, SCN1A (K1580I +5 more)	Single nucleotide variant (missense variant +1 more)	Migraine, familial hemiplegic, 3	GPathogenic
Select item 931569	NM_001165963.4(SCN1A):c.602+3_602+6del	SCN1A	Deletion (splice donor variant)	Migraine, familial hemiplegic, 3 +1 more	GConflicting classifications of pathogenicity
Select item 931547	NM_001165963.4(SCN1A):c.1754G>C (p.Gly585Ala)	SCN1A (G584A +1 more)	Single nucleotide variant (missense variant +2 more)	Migraine, familial hemiplegic, 3	GLikely benign
Select item 931239	NM_001165963.4(SCN1A):c.1922_1923delinsATC (p.Met641fs)	SCN1A (M640fs +1 more)	Indel (frameshift variant +2 more)	Migraine, familial hemiplegic, 3	GLikely pathogenic
Select item 930959	NM_001165963.4(SCN1A):c.941G>A (p.Trp314Ter)	SCN1A (W314*)	Single nucleotide variant (nonsense +2 more)	Migraine, familial hemiplegic, 3	GLikely pathogenic
Select item 930758	NM_001165963.4(SCN1A):c.1843G>T (p.Gly615Ter)	SCN1A (G614* +1 more)	Single nucleotide variant (nonsense +2 more)	Migraine, familial hemiplegic, 3	GPathogenic
Select item 930731	NM_001165963.4(SCN1A):c.4988T>C (p.Leu1663Ser)	LOC102724058, SCN1A (L1634S +5 more)	Single nucleotide variant (missense variant +1 more)	Early infantile epileptic encephalopathy with suppression bursts +1 more	GConflicting classifications of pathogenicity
Select item 930374	NM_001165963.4(SCN1A):c.680T>C (p.Ile227Thr)	SCN1A (I227T)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 930321	NM_001165963.4(SCN1A):c.5341T>C (p.Tyr1781His)	LOC102724058, SCN1A (Y1753H +5 more)	Single nucleotide variant (missense variant +1 more)	Migraine, familial hemiplegic, 3 +1 more	GPathogenic
Select item 930265	NM_001165963.4(SCN1A):c.2177-10_2177-9insA	SCN1A	Insertion (intron variant)	Migraine, familial hemiplegic, 3	GUncertain significance
Select item 894764	NM_001165963.4(SCN1A):c.*677G>A	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 894763	NM_001165963.4(SCN1A):c.*774G>A	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 894731	NM_001165963.4(SCN1A):c.*1325G>A	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Migraine, familial hemiplegic, 3 +1 more	GUncertain significance
Select item 894730	NM_001165963.4(SCN1A):c.*1366A>T	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Migraine, familial hemiplegic, 3 +1 more	GUncertain significance
Select item 894324	NM_001165963.4(SCN1A):c.2508C>T (p.Asp836=)	SCN1A	Single nucleotide variant (synonymous variant +1 more)	Early infantile epileptic encephalopathy with suppression bursts +2 more	GConflicting classifications of pathogenicity
Select item 893908	NM_001165963.4(SCN1A):c.4002G>A (p.Arg1334=)	LOC102724058, SCN1A	Single nucleotide variant (synonymous variant +1 more)	Migraine, familial hemiplegic, 3 +1 more	GUncertain significance
Select item 893876	NM_001165963.4(SCN1A):c.5901C>A (p.Asn1967Lys)	LOC102724058, SCN1A (N1153K +5 more)	Single nucleotide variant (missense variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +1 more	GUncertain significance
Select item 893843	NM_001165963.4(SCN1A):c.*797T>C	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Migraine, familial hemiplegic, 3 +1 more	GUncertain significance
Select item 893842	NM_001165963.4(SCN1A):c.*926C>T	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Migraine, familial hemiplegic, 3 +1 more	GUncertain significance
Select item 893817	NM_001165963.4(SCN1A):c.*1794C>T	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Migraine, familial hemiplegic, 3 +1 more	GUncertain significance
Select item 893727	NM_001165963.4(SCN1A):c.384-5C>T	SCN1A	Single nucleotide variant (intron variant)	Early infantile epileptic encephalopathy with suppression bursts +2 more	GConflicting classifications of pathogenicity
Select item 893690	NM_001165963.4(SCN1A):c.2006C>T (p.Pro669Leu)	SCN1A (P669L +1 more)	Single nucleotide variant (missense variant +3 more)	Early infantile epileptic encephalopathy with suppression bursts +3 more	GUncertain significance
Select item 893618	NM_001165963.4(SCN1A):c.4220G>A (p.Arg1407Gln)	LOC102724058, SCN1A (R1379Q +5 more)	Single nucleotide variant (missense variant +1 more)	Migraine, familial hemiplegic, 3 +2 more	GUncertain significance
Select item 893592	NM_001165963.4(SCN1A):c.*186G>A	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Migraine, familial hemiplegic, 3 +1 more	GUncertain significance
Select item 893591	NM_001165963.4(SCN1A):c.*374T>C	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Migraine, familial hemiplegic, 3 +1 more	GUncertain significance
Select item 893545	NM_001165963.4(SCN1A):c.*1125T>G	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Migraine, familial hemiplegic, 3 +1 more	GUncertain significance
Select item 892842	NM_001165963.4(SCN1A):c.3551-12C>T	LOC102724058, SCN1A	Single nucleotide variant (intron variant)	Migraine, familial hemiplegic, 3 +2 more	GConflicting classifications of pathogenicity
Select item 892780	NM_001165963.4(SCN1A):c.*458G>A	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +1 more	GUncertain significance
Select item 892779	NM_001165963.4(SCN1A):c.*515G>T	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +1 more	GUncertain significance
Select item 892778	NM_001165963.4(SCN1A):c.*553G>A	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +1 more	GUncertain significance
Select item 892750	NM_001165963.4(SCN1A):c.*1144G>C	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +1 more	GUncertain significance
Select item 892749	NM_001165963.4(SCN1A):c.*1152A>G	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +1 more	GUncertain significance
Select item 892748	NM_001165963.4(SCN1A):c.*1297G>A	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +1 more	GUncertain significance
Select item 850219	NM_001165963.4(SCN1A):c.238dup (p.Leu80fs)	SCN1A (L80fs)	Duplication (frameshift variant +2 more)	Early infantile epileptic encephalopathy with suppression bursts	GPathogenic
Select item 839613	NM_001165963.4(SCN1A):c.5092G>A (p.Glu1698Lys)	LOC102724058, SCN1A (E1670K +5 more)	Single nucleotide variant (missense variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +4 more	GUncertain significance
Select item 839612	NM_001165963.4(SCN1A):c.886A>G (p.Ile296Val)	SCN1A (I296V)	Single nucleotide variant (missense variant +2 more)	Early infantile epileptic encephalopathy with suppression bursts +4 more	GConflicting classifications of pathogenicity
Select item 695620	NM_001165963.4(SCN1A):c.2838C>T (p.Arg946=)	SCN1A	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 689733	NM_001165963.4(SCN1A):c.4133A>T (p.Asn1378Ile)	LOC102724058, SCN1A (N1350I +5 more)	Single nucleotide variant (missense variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +2 more	GLikely pathogenic
Select item 682297	NM_001165963.4(SCN1A):c.5656C>A (p.Arg1886=)	LOC102724058, SCN1A	Single nucleotide variant (synonymous variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +3 more	GConflicting classifications of pathogenicity
Select item 672195	NM_001165963.4(SCN1A):c.4095C>T (p.Gly1365=)	LOC102724058, SCN1A	Single nucleotide variant (synonymous variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +3 more	GConflicting classifications of pathogenicity
Select item 626009	NM_001165963.4(SCN1A):c.1343T>C (p.Ile448Thr)	SCN1A (I448T)	Single nucleotide variant (missense variant +2 more)	Early infantile epileptic encephalopathy with suppression bursts +5 more	GUncertain significance
Select item 620251	NM_001165963.4(SCN1A):c.1354A>T (p.Lys452Ter)	SCN1A (K452*)	Single nucleotide variant (nonsense +2 more)	not provided +4 more	GPathogenic
Select item 575324	NM_001165963.4(SCN1A):c.4234A>G (p.Lys1412Glu)	LOC102724058, SCN1A (K1401E +5 more)	Single nucleotide variant (missense variant +1 more)	Migraine, familial hemiplegic, 3 +4 more	GUncertain significance
Select item 574497	NM_001165963.4(SCN1A):c.2234T>G (p.Phe745Cys)	SCN1A (F745C +4 more)	Single nucleotide variant (missense variant +2 more)	Generalized epilepsy with febrile seizures plus, type 2 +2 more	GUncertain significance
Select item 568871	NM_001165963.4(SCN1A):c.542A>G (p.Glu181Gly)	SCN1A (E181G)	Single nucleotide variant (missense variant +2 more)	Early infantile epileptic encephalopathy with suppression bursts +4 more	GUncertain significance
Select item 530625	NM_001165963.4(SCN1A):c.1803C>T (p.Asn601=)	SCN1A	Single nucleotide variant (synonymous variant +2 more)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 530405	NM_001165963.4(SCN1A):c.1753G>C (p.Gly585Arg)	SCN1A (G585R +1 more)	Single nucleotide variant (missense variant +2 more)	Generalized epilepsy with febrile seizures plus, type 2 +3 more	GUncertain significance
Select item 516611	NM_001165963.4(SCN1A):c.606C>T (p.Tyr202=)	SCN1A	Single nucleotide variant (synonymous variant +2 more)	Generalized epilepsy with febrile seizures plus, type 2 +4 more	GConflicting classifications of pathogenicity
Select item 498246	NM_001165963.4(SCN1A):c.5988A>C (p.Lys1996Asn)	LOC102724058, SCN1A (K1985N +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 496124	NM_001165963.4(SCN1A):c.5734C>T (p.Arg1912Ter)	LOC102724058, SCN1A (R1901* +5 more)	Single nucleotide variant (nonsense +1 more)	Migraine, familial hemiplegic, 3 +3 more	GPathogenic
Select item 496120	NM_001165963.4(SCN1A):c.4612G>A (p.Val1538Ile)	LOC102724058, SCN1A (V1527I +5 more)	Single nucleotide variant (missense variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +5 more	GConflicting classifications of pathogenicity
Select item 487362	NM_001165963.4(SCN1A):c.2947-41C>T	SCN1A	Single nucleotide variant (intron variant)	Generalized epilepsy with febrile seizures plus, type 2 +3 more	GBenign
Select item 461281	NM_001165963.4(SCN1A):c.5217C>T (p.Pro1739=)	LOC102724058, SCN1A	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +6 more	GConflicting classifications of pathogenicity
Select item 448247	NM_001165963.4(SCN1A):c.136G>A (p.Glu46Lys)	SCN1A (E46K)	Single nucleotide variant (missense variant +2 more)	Severe myoclonic epilepsy in infancy +5 more	GUncertain significance
Select item 429403	NM_001165963.4(SCN1A):c.3046G>A (p.Val1016Met)	SCN1A (V1005M +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 423837	NM_001165963.4(SCN1A):c.5851G>T (p.Ala1951Ser)	LOC102724058, SCN1A (A1940S +5 more)	Single nucleotide variant (missense variant +1 more)	Migraine, familial hemiplegic, 3 +5 more	GUncertain significance
Select item 384007	NM_001165963.4(SCN1A):c.2649C>T (p.Ile883=)	SCN1A	Single nucleotide variant (synonymous variant +1 more)	Early infantile epileptic encephalopathy with suppression bursts +3 more	GConflicting classifications of pathogenicity
Select item 383462	NM_001165963.4(SCN1A):c.560G>A (p.Arg187Gln)	SCN1A (R187Q)	Single nucleotide variant (missense variant +2 more)	Early infantile epileptic encephalopathy with suppression bursts +3 more	GUncertain significance
Select item 331894	NM_001165963.4(SCN1A):c.565C>G (p.Pro189Ala)	SCN1A (P189A)	Single nucleotide variant (missense variant +2 more)	Early infantile epileptic encephalopathy with suppression bursts +3 more	GUncertain significance
Select item 331893	NM_001165963.4(SCN1A):c.2044-14A>T	SCN1A	Single nucleotide variant (intron variant)	Epilepsy +2 more	GUncertain significance
Select item 331891	NM_001165963.4(SCN1A):c.2176+11A>C	SCN1A	Single nucleotide variant (intron variant)	Migraine, familial hemiplegic, 3 +4 more	GConflicting classifications of pathogenicity
Select item 331890	NM_001165963.4(SCN1A):c.2177-11dup	SCN1A	Duplication (intron variant)	Familial hemiplegic migraine +6 more	GBenign
Select item 331888	NM_001165963.4(SCN1A):c.2459T>C (p.Ile820Thr)	SCN1A (I820T +5 more)	Single nucleotide variant (missense variant +1 more)	Epilepsy +3 more	GUncertain significance
Select item 331887	NM_001165963.4(SCN1A):c.3012T>C (p.Asp1004=)	SCN1A	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +4 more	GConflicting classifications of pathogenicity
Select item 331886	NM_001165963.4(SCN1A):c.3513T>C (p.Pro1171=)	LOC102724058, SCN1A	Single nucleotide variant (non-coding transcript variant +1 more)	Epilepsy +2 more	GUncertain significance
Select item 331885	NM_001165963.4(SCN1A):c.3573T>C (p.Cys1191=)	LOC102724058, SCN1A	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +5 more	GConflicting classifications of pathogenicity
Select item 331884	NM_001165963.4(SCN1A):c.3880-10G>C	LOC102724058, SCN1A	Single nucleotide variant (intron variant)	Migraine, familial hemiplegic, 3 +3 more	GConflicting classifications of pathogenicity
Select item 331883	NM_001165963.4(SCN1A):c.4551A>G (p.Lys1517=)	LOC102724058, SCN1A	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +5 more	GBenign/Likely benign
Select item 331882	NM_001165963.4(SCN1A):c.4581+12C>T	LOC102724058, SCN1A	Single nucleotide variant (intron variant)	Early infantile epileptic encephalopathy with suppression bursts +4 more	GConflicting classifications of pathogenicity
Select item 331881	NM_001165963.4(SCN1A):c.4941A>G (p.Leu1647=)	LOC102724058, SCN1A	Single nucleotide variant (synonymous variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 331880	NM_001165963.4(SCN1A):c.5992G>C (p.Glu1998Gln)	LOC102724058, SCN1A (E1998Q +5 more)	Single nucleotide variant (missense variant +1 more)	Early infantile epileptic encephalopathy with suppression bursts +3 more	GUncertain significance
Select item 331879	NM_001165963.4(SCN1A):c.*129T>G	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Epilepsy +2 more	GUncertain significance
Select item 331877	NM_001165963.4(SCN1A):c.*259T>C	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Epilepsy +2 more	GUncertain significance
Select item 331876	NM_001165963.4(SCN1A):c.*460A>C	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Epilepsy +2 more	GUncertain significance
Select item 331875	NM_001165963.4(SCN1A):c.*588A>G	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +2 more	GBenign/Likely benign
Select item 331873	NM_001165963.4(SCN1A):c.*721A>G	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Generalized epilepsy with febrile seizures plus, type 2 +3 more	GBenign
Select item 331871	NM_001165963.4(SCN1A):c.*912T>A	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Epilepsy +2 more	GUncertain significance
Select item 331870	NM_001165963.4(SCN1A):c.*977T>C	LOC102724058, SCN1A	Single nucleotide variant (3 prime UTR variant +1 more)	Epilepsy +2 more	GUncertain significance

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