ClinVar Miner

List of variants in gene combination LOC110121288, SCN10A reported as likely benign for Brugada syndrome

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_006514.3(SCN10A):c.2816C>T (p.Pro939Leu) rs202174472
NM_006514.3(SCN10A):c.2940C>G (p.Pro980=) rs1192005964
NM_006514.3(SCN10A):c.2972C>T (p.Pro991Leu) rs138413438
NM_006514.3(SCN10A):c.2988T>C (p.Ser996=) rs375913659
NM_006514.3(SCN10A):c.3138G>A (p.Arg1046=) rs371613636
NM_006514.3(SCN10A):c.3237C>T (p.Asp1079=) rs745921364
NM_006514.3(SCN10A):c.3255G>A (p.Glu1085=) rs143610297
NM_006514.3(SCN10A):c.3507+10G>A rs767411176

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