ClinVar Miner

List of variants reported as pathogenic for Andersen Tawil syndrome; Short QT syndrome type 3; Atrial fibrillation, familial, 9

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000891.3(KCNJ2):c.199C>T (p.Arg67Trp)	rs104894580
NM_000891.3(KCNJ2):c.652C>T (p.Arg218Trp)	rs104894578
NM_000891.3(KCNJ2):c.653G>A (p.Arg218Gln)	rs199473384

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