Related gene-specific medical variations for Gene (Select 6717) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1279695	NM_198901.2(SRI):c.7-1315G>C	SRI, SRI-AS1 +1 more	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277351	NM_003130.4(SRI):c.136-150A>C	SRI, SRI-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271507	NM_198901.2(SRI):c.7-1322G>A	SRI, SRI-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262145	NM_198901.2(SRI):c.7-1417_7-1416del	SRI, SRI-AS1	Deletion (intron variant)	not provided	GBenign
Select item 1253279	NM_198901.2(SRI):c.7-1446T>C	SRI, SRI-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234720	NM_003130.4(SRI):c.136-5A>G	SRI, SRI-AS1	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar