ClinVar Miner

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

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 97
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HGVS dbSNP gnomAD frequency
NM_001148.6(ANK2):c.9900C>A (p.Ser3300Arg) rs34270799 0.01986
NM_001148.6(ANK2):c.11218C>A (p.Leu3740Ile) rs35530544 0.01031
NM_001148.6(ANK2):c.9854T>C (p.Ile3285Thr) rs36210417 0.00822
NM_001148.6(ANK2):c.3379+12T>G rs139528815 0.00812
NM_001148.6(ANK2):c.2377-8C>T rs139893914 0.00682
NM_001148.6(ANK2):c.2278-11G>A rs146312675 0.00538
NM_001148.6(ANK2):c.9061G>A (p.Ala3021Thr) rs74348333 0.00465
NM_001148.6(ANK2):c.4744C>T (p.Arg1582Trp) rs35249198 0.00403
NM_001148.6(ANK2):c.9454A>G (p.Thr3152Ala) rs61741040 0.00340
NM_001148.6(ANK2):c.2970A>C (p.Arg990=) rs35956627 0.00336
NM_001148.6(ANK2):c.10861C>G (p.Leu3621Val) rs45570339 0.00327
NM_001148.6(ANK2):c.10395G>A (p.Glu3465=) rs147423696 0.00282
NM_001148.6(ANK2):c.1401A>G (p.Ala467=) rs142159132 0.00269
NM_001148.6(ANK2):c.4152T>C (p.Asp1384=) rs116128106 0.00267
NM_001148.6(ANK2):c.3543C>T (p.Ala1181=) rs76685232 0.00265
NM_001148.6(ANK2):c.3366C>T (p.Asn1122=) rs114896457 0.00256
NM_001148.6(ANK2):c.11791G>A (p.Glu3931Lys) rs45454496 0.00235
NM_001148.6(ANK2):c.6648C>G (p.Gly2216=) rs140926982 0.00208
NM_001148.6(ANK2):c.2277+9C>T rs141965666 0.00205
NM_001148.6(ANK2):c.10371G>A (p.Thr3457=) rs142908806 0.00203
NM_001148.6(ANK2):c.10901T>A (p.Val3634Asp) rs66785829 0.00200
NM_001148.6(ANK2):c.11465G>C (p.Gly3822Ala) rs79577190 0.00178
NM_001148.6(ANK2):c.8354C>T (p.Ser2785Leu) rs145895389 0.00170
NM_001148.6(ANK2):c.3255G>T (p.Ala1085=) rs56173868 0.00156
NM_001148.6(ANK2):c.8658A>G (p.Leu2886=) rs149433267 0.00133
NM_001148.6(ANK2):c.11718G>A (p.Arg3906=) rs35724152 0.00128
NM_001148.6(ANK2):c.11716C>T (p.Arg3906Trp) rs121912706 0.00094
NM_001148.6(ANK2):c.4745G>A (p.Arg1582Gln) rs138842207 0.00090
NM_001148.6(ANK2):c.1863C>G (p.Ser621=) rs146425138 0.00089
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.261G>A (p.Gly87=) rs145502481 0.00064
NM_001148.6(ANK2):c.8979A>G (p.Ile2993Met) rs112252825 0.00064
NM_001148.6(ANK2):c.2900+5135G>A rs139641776 0.00054
NM_001148.6(ANK2):c.130C>G (p.Leu44Val) rs145272651 0.00051
NM_001148.6(ANK2):c.231G>A (p.Val77=) rs149699185 0.00049
NM_001148.6(ANK2):c.198C>T (p.Asn66=) rs146964054 0.00040
NM_001148.6(ANK2):c.2727T>A (p.Thr909=) rs144548535 0.00036
NM_001148.6(ANK2):c.8727C>T (p.Pro2909=) rs144821187 0.00032
NM_001148.6(ANK2):c.9279C>G (p.Thr3093=) rs148851013 0.00026
NM_001148.6(ANK2):c.2868C>T (p.Asn956=) rs145960256 0.00023
NM_001148.6(ANK2):c.10531C>T (p.Leu3511=) rs148462839 0.00022
NM_001148.6(ANK2):c.8388G>A (p.Pro2796=) rs369684289 0.00021
NM_001148.6(ANK2):c.997C>T (p.Leu333=) rs201024064 0.00021
NM_001148.6(ANK2):c.3963T>C (p.Ile1321=) rs72901936 0.00020
NM_001148.6(ANK2):c.6633C>T (p.Ala2211=) rs143516811 0.00018
NM_001148.6(ANK2):c.270G>T (p.Val90=) rs376457094 0.00016
NM_001148.6(ANK2):c.2592T>C (p.Pro864=) rs138641014 0.00015
NM_001148.6(ANK2):c.2249A>G (p.Gln750Arg) rs371787039 0.00014
NM_001148.6(ANK2):c.2850C>A (p.Gly950=) rs189563238 0.00014
NM_001148.6(ANK2):c.4372-7C>T rs370720661 0.00014
NM_001148.6(ANK2):c.11119G>A (p.Asp3707Asn) rs199549660 0.00013
NM_001148.6(ANK2):c.3033C>T (p.Arg1011=) rs142052072 0.00012
NM_001148.6(ANK2):c.4287A>G (p.Ser1429=) rs72556369 0.00011
NM_001148.6(ANK2):c.1899A>G (p.Leu633=) rs377608305 0.00010
NM_001148.6(ANK2):c.8673C>T (p.Pro2891=) rs374884110 0.00010
NM_001148.6(ANK2):c.962G>A (p.Arg321Gln) rs150226540 0.00010
NM_001148.6(ANK2):c.11181C>T (p.Gly3727=) rs185569619 0.00009
NM_001148.6(ANK2):c.2060A>G (p.Asn687Ser) rs29372 0.00009
NM_001148.6(ANK2):c.2127T>C (p.Asn709=) rs113454484 0.00009
NM_001148.6(ANK2):c.2712C>T (p.Ser904=) rs149310669 0.00009
NM_001148.6(ANK2):c.10983T>C (p.Ser3661=) rs544195596 0.00008
NM_001148.6(ANK2):c.11523G>A (p.Pro3841=) rs143290935 0.00007
NM_001148.6(ANK2):c.1135C>T (p.Arg379Cys) rs143043717 0.00006
NM_001148.6(ANK2):c.11628A>G (p.Glu3876=) rs376376716 0.00006
NM_001148.6(ANK2):c.1575G>A (p.Ala525=) rs565952102 0.00006
NM_001148.6(ANK2):c.2679A>G (p.Gly893=) rs766183219 0.00006
NM_001148.6(ANK2):c.8484T>C (p.Asp2828=) rs371140760 0.00006
NM_001148.6(ANK2):c.10032A>G (p.Pro3344=) rs775667097 0.00005
NM_001148.6(ANK2):c.3136C>T (p.Leu1046=) rs149840991 0.00005
NM_001148.6(ANK2):c.813T>C (p.His271=) rs774848857 0.00005
NM_001148.6(ANK2):c.9936C>T (p.Ser3312=) rs758162927 0.00005
NM_001148.6(ANK2):c.1110C>T (p.His370=) rs371839121 0.00004
NM_001148.6(ANK2):c.11864A>G (p.Asn3955Ser) rs201555985 0.00004
NM_001148.6(ANK2):c.1773T>C (p.Ser591=) rs374775005 0.00004
NM_001148.6(ANK2):c.2265C>T (p.Asn755=) rs765273107 0.00004
NM_001148.6(ANK2):c.10707C>T (p.Ile3569=) rs539298479 0.00003
NM_001148.6(ANK2):c.1020C>T (p.Ala340=) rs757576841 0.00002
NM_001148.6(ANK2):c.11586C>T (p.Leu3862=) rs749279759 0.00002
NM_001148.6(ANK2):c.11616C>T (p.Asp3872=) rs768755447 0.00002
NM_001148.6(ANK2):c.1710A>G (p.Ala570=) rs757515084 0.00002
NM_001148.6(ANK2):c.3927A>G (p.Glu1309=) rs567570285 0.00002
NM_001148.6(ANK2):c.615C>T (p.Thr205=) rs587780852 0.00002
NM_001148.6(ANK2):c.10263C>T (p.Ala3421=) rs745900850 0.00001
NM_001148.6(ANK2):c.1803T>C (p.His601=) rs144016063 0.00001
NM_001148.6(ANK2):c.2364C>T (p.Asn788=) rs769405364 0.00001
NM_001148.6(ANK2):c.2819C>G (p.Ala940Gly) rs537484483 0.00001
NM_001148.6(ANK2):c.3882C>T (p.Asn1294=) rs780187690 0.00001
NM_001148.6(ANK2):c.4123-13T>C rs759465783 0.00001
NM_001148.6(ANK2):c.4554C>T (p.Thr1518=) rs747525865 0.00001
NM_001148.6(ANK2):c.8768A>G (p.Gln2923Arg) rs551454026 0.00001
NM_001148.6(ANK2):c.10976G>T (p.Arg3659Leu) rs556640912
NM_001148.6(ANK2):c.11032+20TG[17] rs34201791
NM_001148.6(ANK2):c.2646T>C (p.Asp882=) rs1203137650
NM_001148.6(ANK2):c.4237C>T (p.Leu1413=) rs878854259
NM_001148.6(ANK2):c.4811G>A (p.Arg1604Lys) rs776426910
NM_001148.6(ANK2):c.9474G>T (p.Pro3158=) rs145111737

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