ClinVar Miner

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

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 51
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HGVS dbSNP
NM_001148.6(ANK2):c.10371G>A (p.Thr3457=) rs142908806
NM_001148.6(ANK2):c.10395G>A (p.Glu3465=) rs147423696
NM_001148.6(ANK2):c.10861C>G (p.Leu3621Val) rs45570339
NM_001148.6(ANK2):c.10901T>A (p.Val3634Asp) rs66785829
NM_001148.6(ANK2):c.11181C>T (p.Gly3727=) rs185569619
NM_001148.6(ANK2):c.11218C>A (p.Leu3740Ile) rs35530544
NM_001148.6(ANK2):c.1135C>T (p.Arg379Cys) rs143043717
NM_001148.6(ANK2):c.11538C>T (p.Leu3846=) rs45602336
NM_001148.6(ANK2):c.11716C>T (p.Arg3906Trp) rs121912706
NM_001148.6(ANK2):c.11718G>A (p.Arg3906=) rs35724152
NM_001148.6(ANK2):c.11791G>A (p.Glu3931Lys) rs45454496
NM_001148.6(ANK2):c.1401A>G (p.Ala467=) rs142159132
NM_001148.6(ANK2):c.1899A>G (p.Leu633=) rs377608305
NM_001148.6(ANK2):c.2127T>C (p.Asn709=) rs113454484
NM_001148.6(ANK2):c.2249A>G (p.Gln750Arg) rs371787039
NM_001148.6(ANK2):c.2278-11G>A rs146312675
NM_001148.6(ANK2):c.231G>A (p.Val77=) rs149699185
NM_001148.6(ANK2):c.2377-8C>T rs139893914
NM_001148.6(ANK2):c.2592T>C (p.Pro864=) rs138641014
NM_001148.6(ANK2):c.261G>A (p.Gly87=) rs145502481
NM_001148.6(ANK2):c.2679A>G (p.Gly893=) rs766183219
NM_001148.6(ANK2):c.2712C>T (p.Ser904=) rs149310669
NM_001148.6(ANK2):c.2727T>A (p.Thr909=) rs144548535
NM_001148.6(ANK2):c.2970A>C (p.Arg990=) rs35956627
NM_001148.6(ANK2):c.3136C>T (p.Leu1046=) rs149840991
NM_001148.6(ANK2):c.3543C>T (p.Ala1181=) rs76685232
NM_001148.6(ANK2):c.4152T>C (p.Asp1384=) rs116128106
NM_001148.6(ANK2):c.4372-7C>T rs370720661
NM_001148.6(ANK2):c.4744C>T (p.Arg1582Trp) rs35249198
NM_001148.6(ANK2):c.4745G>A (p.Arg1582Gln) rs138842207
NM_001148.6(ANK2):c.5313G>A (p.Lys1771=) rs140992864
NM_001148.6(ANK2):c.5715G>A (p.Ser1905=) rs143404578
NM_001148.6(ANK2):c.5985G>A (p.Lys1995=) rs116652427
NM_001148.6(ANK2):c.615C>T (p.Thr205=) rs587780852
NM_001148.6(ANK2):c.6648C>G (p.Gly2216=) rs140926982
NM_001148.6(ANK2):c.7059A>G (p.Gln2353=) rs145782226
NM_001148.6(ANK2):c.7117A>G (p.Thr2373Ala) rs184514058
NM_001148.6(ANK2):c.7132G>A (p.Glu2378Lys) rs141191319
NM_001148.6(ANK2):c.7267G>A (p.Ala2423Thr) rs3733616
NM_001148.6(ANK2):c.7488A>G (p.Thr2496=) rs143161930
NM_001148.6(ANK2):c.7831T>C (p.Tyr2611His) rs35338364
NM_001148.6(ANK2):c.7902G>A (p.Val2634=) rs150878494
NM_001148.6(ANK2):c.8388G>A (p.Pro2796=) rs369684289
NM_001148.6(ANK2):c.8673C>T (p.Pro2891=) rs374884110
NM_001148.6(ANK2):c.9061G>A (p.Ala3021Thr) rs74348333
NM_001148.6(ANK2):c.9454A>G (p.Thr3152Ala) rs61741040
NM_001148.6(ANK2):c.962G>A (p.Arg321Gln) rs150226540
NM_001148.6(ANK2):c.9854T>C (p.Ile3285Thr) rs36210417
NM_001148.6(ANK2):c.9900C>A (p.Ser3300Arg) rs34270799
NM_001148.6(ANK2):c.9936C>T (p.Ser3312=) rs758162927
NM_001148.6(ANK2):c.997C>T (p.Leu333=) rs201024064

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