Related gene-specific medical variations for Gene (Select 28234) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 100 of 236

<< First< Prev

Page of 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3165798	NM_019844.4(SLCO1B3):c.97G>A (p.Ala33Thr)	SLCO1B3, SLCO1B3-SLCO1B7 (A5T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165797	NM_019844.4(SLCO1B3):c.745C>T (p.Pro249Ser)	SLCO1B3, SLCO1B3-SLCO1B7 (P249S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165796	NM_019844.4(SLCO1B3):c.646G>A (p.Gly216Arg)	SLCO1B3, SLCO1B3-SLCO1B7 (G188R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165795	NM_019844.4(SLCO1B3):c.1982A>G (p.Asn661Ser)	SLCO1B3, SLCO1B3-SLCO1B7 (N633S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3165794	NM_019844.4(SLCO1B3):c.1180G>A (p.Gly394Arg)	SLCO1B3, SLCO1B3-SLCO1B7 (G366R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165793	NM_019844.4(SLCO1B3):c.1141A>G (p.Ile381Val)	SLCO1B3, SLCO1B3-SLCO1B7 (I353V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165792	NM_019844.4(SLCO1B3):c.1056T>G (p.Phe352Leu)	SLCO1B3, SLCO1B3-SLCO1B7 (F324L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3061660	NM_019844.4(SLCO1B3):c.1863T>C (p.Phe621=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related condition	GLikely benign
Select item 3060445	NM_019844.4(SLCO1B3):c.1672T>C (p.Leu558=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related condition	GLikely benign
Select item 3054796	NM_019844.4(SLCO1B3):c.1866-9T>C	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	SLCO1B3-related condition	GLikely benign
Select item 3052155	NM_019844.4(SLCO1B3):c.1956A>G (p.Gln652=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant +1 more)	SLCO1B3-related condition	GLikely benign
Select item 3051441	NM_019844.4(SLCO1B3):c.840G>A (p.Pro280=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related condition	GLikely benign
Select item 3050120	NM_019844.4(SLCO1B3):c.1714A>G (p.Met572Val)	SLCO1B3, SLCO1B3-SLCO1B7 (M544V +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related condition	GLikely benign
Select item 3050106	NM_019844.4(SLCO1B3):c.1809C>G (p.Ser603=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related condition	GLikely benign
Select item 3048853	NM_019844.4(SLCO1B3):c.1136-13_1136-9del	SLCO1B3, SLCO1B3-SLCO1B7	Deletion (intron variant)	SLCO1B3-related condition	GLikely benign
Select item 3048222	NM_019844.4(SLCO1B3):c.482-10G>T	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	SLCO1B3-related condition	GLikely benign
Select item 3047856	NM_019844.4(SLCO1B3):c.226+5C>T	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	SLCO1B3-related condition	GLikely benign
Select item 3046175	NM_019844.4(SLCO1B3):c.1498-9del	SLCO1B3, SLCO1B3-SLCO1B7	Deletion (intron variant)	SLCO1B3-related condition	GLikely benign
Select item 3045857	NM_019844.4(SLCO1B3):c.1980C>T (p.Asp660=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant +1 more)	SLCO1B3-related condition	GLikely benign
Select item 3045044	NM_019844.4(SLCO1B3):c.153C>T (p.Ser51=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related condition	GLikely benign
Select item 3032943	NM_019844.4(SLCO1B3):c.1290C>T (p.Cys430=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related condition	GLikely benign
Select item 3032765	NM_019844.4(SLCO1B3):c.1328A>G (p.Asp443Gly)	SLCO1B3, SLCO1B3-SLCO1B7 (D415G +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related condition	GUncertain significance
Select item 3032630	NM_019844.4(SLCO1B3):c.948A>G (p.Lys316=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related condition	GLikely benign
Select item 3032507	NM_019844.4(SLCO1B3):c.1068T>C (p.Phe356=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related condition	GLikely benign
Select item 3032132	NM_019844.4(SLCO1B3):c.702C>T (p.Tyr234=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related condition	GLikely benign
Select item 3032033	NM_019844.4(SLCO1B3):c.489A>T (p.Val163=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related condition	GLikely benign
Select item 3031908	NM_019844.4(SLCO1B3):c.1371T>C (p.Ser457=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related condition	GLikely benign
Select item 3031104	NM_019844.4(SLCO1B3):c.300T>C (p.Gly100=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related condition	GLikely benign
Select item 3030685	NM_019844.4(SLCO1B3):c.342A>G (p.Pro114=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related condition	GLikely benign
Select item 3030300	NM_019844.4(SLCO1B3):c.1136-4C>T	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	SLCO1B3-related condition	GLikely benign
Select item 3029790	NM_019844.4(SLCO1B3):c.1827_1830del (p.Gln610fs)	SLCO1B3, SLCO1B3-SLCO1B7 (Q582fs +1 more)	Deletion (frameshift variant)	SLCO1B3-related condition	GUncertain significance
Select item 3029090	NM_019844.4(SLCO1B3):c.1258T>G (p.Leu420Val)	SLCO1B3, SLCO1B3-SLCO1B7 (L392V +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related condition	GLikely benign
Select item 2921058	NM_019844.4(SLCO1B3):c.1732G>C (p.Val578Leu)	SLCO1B3, SLCO1B3-SLCO1B7 (V550L +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2920903	NM_019844.4(SLCO1B3):c.1464A>G (p.Gly488=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	Rotor syndrome	GLikely benign
Select item 2920881	NM_019844.4(SLCO1B3):c.1843A>G (p.Ile615Val)	SLCO1B3, SLCO1B3-SLCO1B7 (I615V +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2920821	NM_019844.4(SLCO1B3):c.1200C>A (p.Phe400Leu)	SLCO1B3, SLCO1B3-SLCO1B7 (F372L +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2636745	NM_019844.4(SLCO1B3):c.485G>A (p.Cys162Tyr)	SLCO1B3, SLCO1B3-SLCO1B7 (C134Y +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related condition	GUncertain significance
Select item 2635830	NM_019844.4(SLCO1B3):c.1226A>G (p.Lys409Arg)	SLCO1B3-SLCO1B7, SLCO1B3 (K381R +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related condition	GUncertain significance
Select item 2634724	NM_019844.4(SLCO1B3):c.143T>C (p.Met48Thr)	SLCO1B3, SLCO1B3-SLCO1B7 (M20T +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related condition	GUncertain significance
Select item 2634168	NM_019844.4(SLCO1B3):c.482-6C>A	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	SLCO1B3-related condition	GUncertain significance
Select item 2633485	NM_019844.4(SLCO1B3):c.1825G>A (p.Ala609Thr)	SLCO1B3, SLCO1B3-SLCO1B7 (A581T +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related condition	GUncertain significance
Select item 2632059	NM_019844.4(SLCO1B3):c.1720T>C (p.Phe574Leu)	SLCO1B3, SLCO1B3-SLCO1B7 (F546L +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related condition	GUncertain significance
Select item 2631904	NM_019844.4(SLCO1B3):c.1123A>C (p.Asn375His)	SLCO1B3, SLCO1B3-SLCO1B7 (N347H +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related condition	GUncertain significance
Select item 2629244	NM_019844.4(SLCO1B3):c.763G>C (p.Val255Leu)	SLCO1B3, SLCO1B3-SLCO1B7 (V227L +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related condition	GUncertain significance
Select item 2620875	NM_019844.4(SLCO1B3):c.1997T>C (p.Met666Thr)	SLCO1B3, SLCO1B3-SLCO1B7 (M666T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2585172	NM_019844.4(SLCO1B3):c.83A>C (p.Lys28Thr)	SLCO1B3, SLCO1B3-SLCO1B7 (K28T)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2543360	NM_019844.4(SLCO1B3):c.647G>T (p.Gly216Val)	SLCO1B3, SLCO1B3-SLCO1B7 (G188V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536184	NM_019844.4(SLCO1B3):c.4G>A (p.Asp2Asn)	SLCO1B3, SLCO1B3-SLCO1B7 (D2N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515453	NM_019844.4(SLCO1B3):c.1615G>C (p.Ala539Pro)	SLCO1B3, SLCO1B3-SLCO1B7 (A511P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511599	NM_019844.4(SLCO1B3):c.292G>C (p.Gly98Arg)	SLCO1B3, SLCO1B3-SLCO1B7 (G98R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495124	NM_019844.4(SLCO1B3):c.1730T>A (p.Met577Lys)	SLCO1B3, SLCO1B3-SLCO1B7 (M577K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491157	NM_019844.4(SLCO1B3):c.1987A>G (p.Arg663Gly)	SLCO1B3, SLCO1B3-SLCO1B7 (R635G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470180	NM_019844.4(SLCO1B3):c.697A>C (p.Met233Leu)	SLCO1B3, SLCO1B3-SLCO1B7 (M233L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2442029	NM_019844.4(SLCO1B3):c.587T>C (p.Ile196Thr)	SLCO1B3, SLCO1B3-SLCO1B7 (I168T +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2436109	NM_019844.4(SLCO1B3):c.1274A>G (p.Tyr425Cys)	SLCO1B3, SLCO1B3-SLCO1B7 (Y397C +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2436108	NM_019844.4(SLCO1B3):c.1205T>C (p.Leu402Ser)	SLCO1B3, SLCO1B3-SLCO1B7 (L374S +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome +1 more	GUncertain significance
Select item 2436107	NM_019844.4(SLCO1B3):c.1685T>C (p.Ile562Thr)	SLCO1B3, SLCO1B3-SLCO1B7 (I534T +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2436106	NM_019844.4(SLCO1B3):c.446_448del (p.Ser149del)	SLCO1B3, SLCO1B3-SLCO1B7 (S121del +1 more)	Deletion (inframe_deletion)	Rotor syndrome +1 more	GUncertain significance
Select item 2436105	NM_019844.4(SLCO1B3):c.1363C>G (p.Pro455Ala)	SLCO1B3, SLCO1B3-SLCO1B7 (P427A +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2436104	NM_019844.4(SLCO1B3):c.1241C>A (p.Thr414Asn)	SLCO1B3, SLCO1B3-SLCO1B7 (T386N +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2436102	NM_019844.4(SLCO1B3):c.956C>G (p.Thr319Ser)	SLCO1B3, SLCO1B3-SLCO1B7 (T291S +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2436101	NM_019844.4(SLCO1B3):c.67C>T (p.Arg23Cys)	SLCO1B3, SLCO1B3-SLCO1B7 (R23C)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2436100	NM_019844.4(SLCO1B3):c.1291G>A (p.Glu431Lys)	SLCO1B3, SLCO1B3-SLCO1B7 (E403K +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2436099	NM_019844.4(SLCO1B3):c.2020T>A (p.Leu674Ile)	SLCO1B3, SLCO1B3-SLCO1B7 (L646I +1 more)	Single nucleotide variant (missense variant +1 more)	Rotor syndrome	GUncertain significance
Select item 2436098	NM_019844.4(SLCO1B3):c.1147A>G (p.Ile383Val)	SLCO1B3, SLCO1B3-SLCO1B7 (I355V +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome +1 more	GUncertain significance
Select item 2436097	NM_019844.4(SLCO1B3):c.170_174del (p.Arg57fs)	SLCO1B3, SLCO1B3-SLCO1B7 (R29fs +1 more)	Deletion (frameshift variant)	Rotor syndrome	GUncertain significance
Select item 2436096	NM_019844.4(SLCO1B3):c.1364C>G (p.Pro455Arg)	SLCO1B3, SLCO1B3-SLCO1B7 (P427R +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 2436095	NM_019844.4(SLCO1B3):c.2105A>G (p.Asn702Ser)	SLCO1B3, SLCO1B3-SLCO1B7 (N674S +1 more)	Single nucleotide variant (missense variant +1 more)	Rotor syndrome +1 more	GUncertain significance
Select item 2428609	NM_019844.4(SLCO1B3):c.263G>T (p.Gly88Val)	SLCO1B3, SLCO1B3-SLCO1B7 (G60V +1 more)	Single nucleotide variant (missense variant)	SLCO1B3-related condition +1 more	GUncertain significance
Select item 2428520	NM_019844.4(SLCO1B3):c.481+7A>G	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	Rotor syndrome	GLikely benign
Select item 2411382	NM_019844.4(SLCO1B3):c.722A>T (p.Asp241Val)	SLCO1B3, SLCO1B3-SLCO1B7 (D213V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398052	NM_019844.4(SLCO1B3):c.2041G>A (p.Val681Ile)	SLCO1B3, SLCO1B3-SLCO1B7 (V653I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2385114	NM_019844.4(SLCO1B3):c.1102G>A (p.Gly368Ser)	SLCO1B3, SLCO1B3-SLCO1B7 (G368S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320409	NM_019844.4(SLCO1B3):c.130G>A (p.Gly44Ser)	SLCO1B3, SLCO1B3-SLCO1B7 (G16S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292114	NM_019844.4(SLCO1B3):c.676C>A (p.Leu226Met)	SLCO1B3, SLCO1B3-SLCO1B7 (L198M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274630	NM_019844.4(SLCO1B3):c.778C>A (p.Leu260Ile)	SLCO1B3, SLCO1B3-SLCO1B7 (L232I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245646	NM_019844.4(SLCO1B3):c.1334A>G (p.Asn445Ser)	SLCO1B3, SLCO1B3-SLCO1B7 (N445S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235803	NM_019844.4(SLCO1B3):c.1480G>C (p.Gly494Arg)	SLCO1B3, SLCO1B3-SLCO1B7 (G466R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211464	NM_019844.4(SLCO1B3):c.537G>A (p.Met179Ile)	SLCO1B3, SLCO1B3-SLCO1B7 (M151I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209592	NM_019844.4(SLCO1B3):c.2090A>G (p.Asp697Gly)	SLCO1B3, SLCO1B3-SLCO1B7 (D669G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1330934	NM_019844.4(SLCO1B3):c.1135+1G>A	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (splice donor variant)	Rotor syndrome	GPathogenic
Select item 1330928	NM_019844.4(SLCO1B3):c.1637dup (p.Leu546fs)	SLCO1B3, SLCO1B3-SLCO1B7 (L518fs +1 more)	Duplication (frameshift variant)	SLCO1B3-related condition +1 more	GConflicting classifications of pathogenicity
Select item 1330853	NM_019844.4(SLCO1B3):c.264A>C (p.Gly88=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant)	SLCO1B3-related condition +1 more	GLikely benign
Select item 1330844	NM_019844.4(SLCO1B3):c.1974A>C (p.Ala658=)	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (synonymous variant +1 more)	Rotor syndrome	GLikely benign
Select item 1330526	NM_019844.4(SLCO1B3):c.481+3A>G	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	Rotor syndrome	GLikely benign
Select item 1330435	NM_019844.4(SLCO1B3):c.227G>T (p.Gly76Val)	SLCO1B3, SLCO1B3-SLCO1B7 (G48V +1 more)	Single nucleotide variant (missense variant)	Rotor syndrome	GUncertain significance
Select item 1330411	NM_019844.4(SLCO1B3):c.481+12_481+25del	SLCO1B3, SLCO1B3-SLCO1B7	Deletion (intron variant)	Rotor syndrome	GLikely benign
Select item 1297898	NM_019844.4(SLCO1B3):c.629-80A>G	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295238	NM_019844.4(SLCO1B3):c.1136-197C>T	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287831	NM_019844.4(SLCO1B3):c.482-141C>A	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287231	NM_019844.4(SLCO1B3):c.227-63T>C	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287212	NM_019844.4(SLCO1B3):c.84+124A>T	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286908	NM_019844.4(SLCO1B3):c.1498-82T>G	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286427	NM_019844.4(SLCO1B3):c.359+76G>A	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280289	NM_019844.4(SLCO1B3):c.482-300C>G	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276630	NM_019844.4(SLCO1B3):c.1135+150A>G	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274436	NM_019844.4(SLCO1B3):c.84+72C>T	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271029	NM_019844.4(SLCO1B3):c.1498-250A>G	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268707	NM_019844.4(SLCO1B3):c.481+271C>T	SLCO1B3, SLCO1B3-SLCO1B7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265202	NM_019844.4(SLCO1B3):c.1682+250_1682+253del	SLCO1B3, SLCO1B3-SLCO1B7	Deletion (intron variant)	not provided	GBenign

<< First< Prev

Page of 3