ClinVar Miner

List of variants in gene SCN3B studied for atrial fibrillation, familial, 16

Included ClinVar conditions (1):
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Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_001040151.2(SCN3B):c.29T>C (p.Leu10Pro) rs121918282 0.00036
NM_001040151.2(SCN3B):c.389C>T (p.Ala130Val) rs587777556 0.00001
NM_001040151.2(SCN3B):c.17G>A (p.Arg6Lys) rs587777558
NM_001040151.2(SCN3B):c.482T>C (p.Met161Thr) rs587777557

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