ClinVar Miner

List of variants reported as likely benign for atrial fibrillation, familial, 9

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_000891.3(KCNJ2):c.*1596A>C rs117409545 0.02347
NM_000891.3(KCNJ2):c.-163_-162insTC rs61077847 0.02248
NM_000891.3(KCNJ2):c.-162_-161insGAGTAGT rs58144126 0.02246
NM_000891.3(KCNJ2):c.*1350G>A rs116077770 0.00360
NM_000891.3(KCNJ2):c.1229A>G (p.Asn410Ser) rs141069645 0.00042
NM_000891.3(KCNJ2):c.*1125G>A rs191729421 0.00033
NM_000891.3(KCNJ2):c.-2C>T rs144760658 0.00013

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