ClinVar Miner

List of variants in gene ANK2 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Gene type:
ClinVar version:
Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_001148.6(ANK2):c.9854T>C (p.Ile3285Thr) rs36210417 0.00822
NM_001148.6(ANK2):c.11791G>A (p.Glu3931Lys) rs45454496 0.00235
NM_001148.6(ANK2):c.10901T>A (p.Val3634Asp) rs66785829 0.00200
NM_001148.6(ANK2):c.8354C>T (p.Ser2785Leu) rs145895389 0.00170
NM_001148.6(ANK2):c.11231C>A (p.Thr3744Asn) rs121912705 0.00077
NM_001148.6(ANK2):c.11459G>A (p.Arg3820Gln) rs138085317 0.00067
NM_001148.6(ANK2):c.9046G>A (p.Glu3016Lys) rs149963885 0.00052
NM_001148.6(ANK2):c.9923C>G (p.Thr3308Ser) rs145145511 0.00051
NM_001148.6(ANK2):c.9526G>T (p.Asp3176Tyr) rs138928206 0.00018
NM_001148.6(ANK2):c.3074G>C (p.Gly1025Ala) rs773532854 0.00010
NM_001148.6(ANK2):c.2060A>G (p.Asn687Ser) rs29372 0.00009
NM_001148.6(ANK2):c.6641C>T (p.Pro2214Leu) rs143469039 0.00009
NM_001148.6(ANK2):c.10322G>A (p.Arg3441Gln) rs772954896 0.00007
NM_001148.6(ANK2):c.3931G>A (p.Val1311Ile) rs34065266 0.00007
NM_001148.6(ANK2):c.4016C>T (p.Pro1339Leu) rs371357815 0.00007
NM_001148.6(ANK2):c.8324A>G (p.His2775Arg) rs534934297 0.00006
NM_001148.6(ANK2):c.4254C>T (p.Arg1418=) rs778974823 0.00005
NM_001148.6(ANK2):c.2622A>G (p.Ser874=) rs764486532 0.00004
NM_001148.6(ANK2):c.2964G>T (p.Gly988=) rs779092487 0.00004
NM_001148.6(ANK2):c.2289G>A (p.Thr763=) rs753131867 0.00001
NM_001148.6(ANK2):c.2364C>T (p.Asn788=) rs769405364 0.00001
NM_001148.6(ANK2):c.3090G>T (p.Leu1030=) rs1487758535 0.00001
NM_001148.6(ANK2):c.4372-8G>A rs771323413 0.00001
NM_001148.6(ANK2):c.6627G>T (p.Gly2209=) rs755239682 0.00001
NM_001148.6(ANK2):c.8409A>G (p.Glu2803=) rs74743698 0.00001
NM_001148.6(ANK2):c.9598C>T (p.Leu3200Phe) rs750774547 0.00001
NM_001148.6(ANK2):c.10362G>C (p.Arg3454Ser) rs55726422
NM_001148.6(ANK2):c.10734T>C (p.Asp3578=)
NM_001148.6(ANK2):c.10962A>G (p.Glu3654=) rs1564112382
NM_001148.6(ANK2):c.11032+19delinsGTG rs2096464205
NM_001148.6(ANK2):c.11032+8TG[6] rs749676836
NM_001148.6(ANK2):c.11262A>G (p.Ser3754=) rs780604005
NM_001148.6(ANK2):c.3255G>A (p.Ala1085=) rs56173868
NM_001148.6(ANK2):c.4695C>T (p.Ile1565=)

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