ClinVar Miner

Variants in gene ANK2 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 34
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HGVS dbSNP
NM_001148.6(ANK2):c.10118C>T (p.Ala3373Val) rs371358639
NM_001148.6(ANK2):c.10362G>C (p.Arg3454Ser) rs55726422
NM_001148.6(ANK2):c.10861C>G (p.Leu3621Val) rs45570339
NM_001148.6(ANK2):c.11198_11200del (p.Gly3733del) rs730880049
NM_001148.6(ANK2):c.11231C>A (p.Thr3744Asn) rs121912705
NM_001148.6(ANK2):c.11538C>T (p.Leu3846=) rs45602336
NM_001148.6(ANK2):c.11594A>G (p.Asp3865Gly) rs140606121
NM_001148.6(ANK2):c.11716C>T (p.Arg3906Trp) rs121912706
NM_001148.6(ANK2):c.1177G>A (p.Ala393Thr) rs147458476
NM_001148.6(ANK2):c.11791G>A (p.Glu3931Lys) rs45454496
NM_001148.6(ANK2):c.130C>G (p.Leu44Val) rs145272651
NM_001148.6(ANK2):c.1783-4A>G rs755543636
NM_001148.6(ANK2):c.3074G>C (p.Gly1025Ala) rs773532854
NM_001148.6(ANK2):c.3255G>A (p.Ala1085=) rs56173868
NM_001148.6(ANK2):c.3931G>A (p.Val1311Ile) rs34065266
NM_001148.6(ANK2):c.4016C>T (p.Pro1339Leu) rs371357815
NM_001148.6(ANK2):c.4315G>T (p.Gly1439Cys) rs34591340
NM_001148.6(ANK2):c.4456G>C (p.Val1486Leu) rs149678604
NM_001148.6(ANK2):c.4782T>G (p.Ile1594Met) rs775386505
NM_001148.6(ANK2):c.5231C>A (p.Ala1744Asp) rs147706514
NM_001148.6(ANK2):c.5758G>A (p.Gly1920Arg) rs140189724
NM_001148.6(ANK2):c.6228G>T (p.Lys2076Asn) rs144848998
NM_001148.6(ANK2):c.669+3A>G rs370475820
NM_001148.6(ANK2):c.6854T>C (p.Ile2285Thr) rs150684838
NM_001148.6(ANK2):c.6973G>C (p.Asp2325His) rs1298469624
NM_001148.6(ANK2):c.7132G>A (p.Glu2378Lys) rs141191319
NM_001148.6(ANK2):c.7183A>C (p.Thr2395Pro) rs201693280
NM_001148.6(ANK2):c.7236A>T (p.Ala2412=) rs1394535709
NM_001148.6(ANK2):c.7436A>G (p.Lys2479Arg) rs201619005
NM_001148.6(ANK2):c.8843C>G (p.Ala2948Gly) rs138438183
NM_001148.6(ANK2):c.8892C>G (p.Ile2964Met) rs62313245
NM_001148.6(ANK2):c.9526G>T (p.Asp3176Tyr) rs138928206
NM_001148.6(ANK2):c.962G>A (p.Arg321Gln) rs150226540
NM_001148.6(ANK2):c.9825T>G (p.Asp3275Glu) rs149043752

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