ClinVar Miner

List of variants reported as likely benign for Brugada syndrome by Biesecker Lab/Clinical Genomics Section,National Institutes of Health

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_000335.4(SCN5A):c.3875T>C (p.Phe1292Ser) rs41311127
NM_000335.4(SCN5A):c.5491C>G (p.Gln1831Glu) rs199473320
NM_000335.4(SCN5A):c.5848G>T (p.Val1950Leu) rs41315493
NM_005472.4(KCNE3):c.296G>A (p.Arg99His) rs121908441
NM_172057.2(KCNH2):c.1597G>A (p.Gly533Ser) rs41314354

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