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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3322643	NM_003130.4(SRI):c.34G>A (p.Gly12Arg)	LOC129998765, SRI +1 more (G12R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1279695	NM_198901.2(SRI):c.7-1315G>C	SRI, LOC129998765 +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-AS1, SRI	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