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: 93
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HGVS dbSNP gnomAD frequency
NM_001148.6(ANK2):c.10861C>G (p.Leu3621Val) rs45570339 0.00327
NM_001148.6(ANK2):c.11791G>A (p.Glu3931Lys) rs45454496 0.00235
NM_001148.6(ANK2):c.4373A>G (p.Glu1458Gly) rs72544141 0.00085
NM_001148.6(ANK2):c.11538C>T (p.Leu3846=) rs45602336 0.00084
NM_001148.6(ANK2):c.11231C>A (p.Thr3744Asn) rs121912705 0.00077
NM_001148.6(ANK2):c.669+3A>G rs370475820 0.00072
NM_001148.6(ANK2):c.4456G>C (p.Val1486Leu) rs149678604 0.00068
NM_001148.6(ANK2):c.10881T>G (p.His3627Gln) rs148405740 0.00029
NM_001148.6(ANK2):c.11009C>A (p.Thr3670Asn) rs45608232 0.00029
NM_001148.6(ANK2):c.9825T>G (p.Asp3275Glu) rs149043752 0.00029
NM_001148.6(ANK2):c.1910C>T (p.Ala637Val) rs150488571 0.00028
NM_001148.6(ANK2):c.8843C>G (p.Ala2948Gly) rs138438183 0.00027
NM_001148.6(ANK2):c.10703G>A (p.Arg3568Gln) rs142612379 0.00023
NM_001148.6(ANK2):c.4315G>T (p.Gly1439Cys) rs34591340 0.00023
NM_001148.6(ANK2):c.9424A>C (p.Thr3142Pro) rs374350634 0.00023
NM_001148.6(ANK2):c.4310C>T (p.Thr1437Met) rs142534126 0.00019
NM_001148.6(ANK2):c.8463C>A (p.Asp2821Glu) rs780668435 0.00019
NM_001148.6(ANK2):c.2836C>T (p.Arg946Cys) rs200524407 0.00018
NM_001148.6(ANK2):c.8116G>C (p.Glu2706Gln) rs142652341 0.00018
NM_001148.6(ANK2):c.9526G>T (p.Asp3176Tyr) rs138928206 0.00018
NM_001148.6(ANK2):c.9682G>A (p.Val3228Met) rs141013157 0.00016
NM_001148.6(ANK2):c.2110C>G (p.Gln704Glu) rs139197937 0.00014
NM_001148.6(ANK2):c.11119G>A (p.Asp3707Asn) rs199549660 0.00013
NM_001148.6(ANK2):c.8239C>T (p.Arg2747Cys) rs376628082 0.00013
NM_001148.6(ANK2):c.8892C>G (p.Ile2964Met) rs62313245 0.00013
NM_001148.6(ANK2):c.9853A>C (p.Ile3285Leu) rs144603824 0.00012
NM_001148.6(ANK2):c.1673T>C (p.Leu558Ser) rs139199018 0.00011
NM_001148.6(ANK2):c.8144C>T (p.Ser2715Phe) rs147619875 0.00011
NM_001148.6(ANK2):c.9841C>G (p.Gln3281Glu) rs372534074 0.00011
NM_001148.6(ANK2):c.10627A>G (p.Ile3543Val) rs753102215 0.00010
NM_001148.6(ANK2):c.10805G>A (p.Arg3602Gln) rs374991526 0.00010
NM_001148.6(ANK2):c.3074G>C (p.Gly1025Ala) rs773532854 0.00010
NM_001148.6(ANK2):c.9116A>G (p.Asp3039Gly) rs140539843 0.00010
NM_001148.6(ANK2):c.1136G>T (p.Arg379Leu) rs186264035 0.00009
NM_001148.6(ANK2):c.2060A>G (p.Asn687Ser) rs29372 0.00009
NM_001148.6(ANK2):c.877G>A (p.Asp293Asn) rs752213208 0.00009
NM_001148.6(ANK2):c.11470C>G (p.Pro3824Ala) rs747961230 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.6505G>A (p.Val2169Ile) rs149292242 0.00007
NM_001148.6(ANK2):c.8166G>A (p.Met2722Ile) rs193922637 0.00007
NM_001148.6(ANK2):c.10016C>T (p.Ala3339Val) rs150437645 0.00006
NM_001148.6(ANK2):c.11354A>G (p.Gln3785Arg) rs150808807 0.00006
NM_001148.6(ANK2):c.4982A>G (p.Lys1661Arg) rs761759361 0.00006
NM_001148.6(ANK2):c.8176A>G (p.Thr2726Ala) rs781344591 0.00006
NM_001148.6(ANK2):c.8324A>G (p.His2775Arg) rs534934297 0.00006
NM_001148.6(ANK2):c.85-5C>T rs372560419 0.00006
NM_001148.6(ANK2):c.9916G>A (p.Val3306Ile) rs200922244 0.00006
NM_001148.6(ANK2):c.1177G>A (p.Ala393Thr) rs147458476 0.00005
NM_001148.6(ANK2):c.5063A>G (p.Gln1688Arg) rs369680021 0.00005
NM_001148.6(ANK2):c.8387C>T (p.Pro2796Leu) rs182956726 0.00005
NM_001148.6(ANK2):c.8918T>G (p.Val2973Gly) rs142302291 0.00005
NM_001148.6(ANK2):c.10503A>G (p.Ile3501Met) rs370472530 0.00004
NM_001148.6(ANK2):c.10945A>G (p.Met3649Val) rs145856327 0.00004
NM_001148.6(ANK2):c.1773T>C (p.Ser591=) rs374775005 0.00004
NM_001148.6(ANK2):c.8041C>G (p.Leu2681Val) rs1489919946 0.00004
NM_001148.6(ANK2):c.9679A>C (p.Thr3227Pro) rs140604600 0.00004
NM_001148.6(ANK2):c.11594A>G (p.Asp3865Gly) rs140606121 0.00003
NM_001148.6(ANK2):c.4122+4C>A rs756374268 0.00003
NM_001148.6(ANK2):c.4912A>G (p.Asn1638Asp) rs748573794 0.00003
NM_001148.6(ANK2):c.8417T>C (p.Val2806Ala) rs769091762 0.00003
NM_001148.6(ANK2):c.10118C>T (p.Ala3373Val) rs371358639 0.00002
NM_001148.6(ANK2):c.11182G>A (p.Val3728Ile) rs773907372 0.00002
NM_001148.6(ANK2):c.11652A>G (p.Glu3884=) rs752145926 0.00002
NM_001148.6(ANK2):c.2160T>A (p.Asp720Glu) rs748835902 0.00002
NM_001148.6(ANK2):c.3067G>A (p.Gly1023Arg) rs151127289 0.00002
NM_001148.6(ANK2):c.8182G>A (p.Glu2728Lys) rs756424757 0.00002
NM_001148.6(ANK2):c.8927C>G (p.Ser2976Cys) rs371343942 0.00002
NM_001148.6(ANK2):c.9703C>T (p.Pro3235Ser) rs202098889 0.00002
NM_001148.6(ANK2):c.9842A>G (p.Gln3281Arg) rs1306812632 0.00002
NM_001148.6(ANK2):c.10573G>A (p.Glu3525Lys) rs781552524 0.00001
NM_001148.6(ANK2):c.1252G>A (p.Val418Met) rs760073103 0.00001
NM_001148.6(ANK2):c.1783-4A>G rs755543636 0.00001
NM_001148.6(ANK2):c.1986A>G (p.Gly662=) rs765012746 0.00001
NM_001148.6(ANK2):c.4687A>C (p.Asn1563His) rs1476737595 0.00001
NM_001148.6(ANK2):c.56G>A (p.Ser19Asn) rs369260005 0.00001
NM_001148.6(ANK2):c.8057T>C (p.Val2686Ala) rs56095304 0.00001
NM_001148.6(ANK2):c.8447G>A (p.Gly2816Asp) rs199538455 0.00001
NM_001148.6(ANK2):c.10362G>C (p.Arg3454Ser) rs55726422
NM_001148.6(ANK2):c.10685C>T (p.Pro3562Leu) rs779374859
NM_001148.6(ANK2):c.10976G>A (p.Arg3659His) rs556640912
NM_001148.6(ANK2):c.10976G>T (p.Arg3659Leu) rs556640912
NM_001148.6(ANK2):c.11198_11200del (p.Gly3733del) rs730880049
NM_001148.6(ANK2):c.11522C>T (p.Pro3841Leu) rs767769233
NM_001148.6(ANK2):c.2460CAC[4] (p.Thr826del) rs770530257
NM_001148.6(ANK2):c.3255G>A (p.Ala1085=) rs56173868
NM_001148.6(ANK2):c.4371+19T>C rs1057522286
NM_001148.6(ANK2):c.4555G>T (p.Ala1519Ser) rs200920714
NM_001148.6(ANK2):c.4940G>A (p.Cys1647Tyr) rs2095548237
NM_001148.6(ANK2):c.8140G>A (p.Val2714Ile) rs753223319
NM_001148.6(ANK2):c.8381A>G (p.Gln2794Arg) rs528909081
NM_001148.6(ANK2):c.9590A>G (p.Asp3197Gly)
NM_001148.6(ANK2):c.9991T>C (p.Ser3331Pro)

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