ClinVar Miner

List of variants in gene ANK2 reported by Stanford Center for Inherited Cardiovascular Disease, Stanford University

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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_001148.6(ANK2):c.11231C>A (p.Thr3744Asn) rs121912705 0.00077
NM_001148.6(ANK2):c.9046G>A (p.Glu3016Lys) rs149963885 0.00052
NM_001148.6(ANK2):c.4315G>T (p.Gly1439Cys) rs34591340 0.00023
NM_001148.6(ANK2):c.4310C>T (p.Thr1437Met) rs142534126 0.00019
NM_001148.6(ANK2):c.9526G>T (p.Asp3176Tyr) rs138928206 0.00018
NM_001148.6(ANK2):c.11354A>G (p.Gln3785Arg) rs150808807 0.00006
NM_001148.6(ANK2):c.10147G>A (p.Ala3383Thr) rs374257100 0.00003
NM_001148.6(ANK2):c.1118C>T (p.Ala373Val) rs772102642 0.00003
NM_001148.6(ANK2):c.11134G>A (p.Val3712Ile) rs146476345 0.00002
NM_001148.6(ANK2):c.2713G>A (p.Asp905Asn) rs759275920 0.00002
NM_001148.6(ANK2):c.2063T>A (p.Ile688Asn) rs746436835 0.00001
NM_001148.6(ANK2):c.2987G>A (p.Arg996Gln) rs200124480 0.00001
NM_001148.6(ANK2):c.9427C>G (p.Leu3143Val) rs776074680 0.00001
NM_001148.6(ANK2):c.9880A>C (p.Asn3294His) rs763211298 0.00001
NM_001148.6(ANK2):c.2280C>G (p.Asn760Lys) rs1060501162
NM_001148.6(ANK2):c.2460CAC[4] (p.Thr826del) rs770530257
NM_001148.6(ANK2):c.9511T>G (p.Ser3171Ala) rs1554569481

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