ClinVar Miner

List of variants in gene ANK2 reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 100
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HGVS dbSNP gnomAD frequency
NM_001148.6(ANK2):c.11673T>C (p.His3891=) rs2293324 0.30277
NM_001148.6(ANK2):c.3579C>T (p.Arg1193=) rs3736575 0.23645
NM_001148.6(ANK2):c.3893+14G>T rs2272231 0.21141
NM_001148.6(ANK2):c.8503C>T (p.Pro2835Ser) rs3733617 0.14405
NM_001148.6(ANK2):c.9648A>G (p.Glu3216=) rs10013743 0.12780
NM_001148.6(ANK2):c.10888+20C>T rs35728190 0.10852
NM_001148.6(ANK2):c.2337C>T (p.Val779=) rs29341 0.03480
NM_001148.4(ANK2):c.*7C>T rs35446871 0.03095
NM_001148.6(ANK2):c.3510A>G (p.Val1170=) rs35336373 0.02906
NM_001148.6(ANK2):c.384+19C>T rs45502093 0.02751
NM_001148.6(ANK2):c.9900C>A (p.Ser3300Arg) rs34270799 0.01986
NM_001148.6(ANK2):c.6634G>A (p.Gly2212Ser) rs61734478 0.01567
NM_001148.6(ANK2):c.11218C>A (p.Leu3740Ile) rs35530544 0.01031
NM_001148.6(ANK2):c.11790C>T (p.Ile3930=) rs45517840 0.00954
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.9996T>C (p.Ser3332=) rs145557320 0.00778
NM_001148.6(ANK2):c.2377-8C>T rs139893914 0.00682
NM_001148.6(ANK2):c.2178+18C>T rs45447896 0.00674
NM_001148.6(ANK2):c.1881+8C>G rs74976371 0.00612
NM_001148.6(ANK2):c.1995A>G (p.Pro665=) rs45442693 0.00612
NM_001148.6(ANK2):c.1245A>G (p.Glu415=) rs34145832 0.00608
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.4404+16T>C rs2272233 0.00409
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.9286A>G (p.Ser3096Gly) rs144158934 0.00238
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.11860-18T>G rs138978479 0.00207
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.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.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.11538C>T (p.Leu3846=) rs45602336 0.00084
NM_001148.6(ANK2):c.11694+19T>A rs114122425 0.00066
NM_001148.6(ANK2):c.261G>A (p.Gly87=) rs145502481 0.00064
NM_001148.6(ANK2):c.2900+5135G>A rs139641776 0.00054
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.4123-19T>G rs199938838 0.00035
NM_001148.6(ANK2):c.8727C>T (p.Pro2909=) rs144821187 0.00032
NM_001148.6(ANK2):c.741C>T (p.Asn247=) rs190102899 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.-18C>G rs201646790 0.00019
NM_001148.6(ANK2):c.6633C>T (p.Ala2211=) rs143516811 0.00018
NM_001148.6(ANK2):c.11032+19A>G rs200769962 0.00016
NM_001148.6(ANK2):c.2080-18G>T rs199937888 0.00016
NM_001148.6(ANK2):c.2592T>C (p.Pro864=) rs138641014 0.00015
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.4287A>G (p.Ser1429=) rs72556369 0.00011
NM_001148.6(ANK2):c.792+15A>G rs375914552 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.2060A>G (p.Asn687Ser) rs29372 0.00009
NM_001148.6(ANK2):c.3507T>C (p.Gly1169=) rs200262333 0.00008
NM_001148.6(ANK2):c.3224+7G>A rs376534098 0.00007
NM_001148.6(ANK2):c.-39G>T rs372870729 0.00006
NM_001148.6(ANK2):c.11628A>G (p.Glu3876=) rs376376716 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.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.2901-16C>G rs200750637 0.00004
NM_001148.6(ANK2):c.9153C>T (p.Asp3051=) rs144397802 0.00004
NM_001148.6(ANK2):c.2548+18T>C rs200150276 0.00003
NM_001148.6(ANK2):c.1485+19A>G rs3025731 0.00002
NM_001148.6(ANK2):c.1680C>T (p.Thr560=) rs752903781 0.00002
NM_001148.6(ANK2):c.615C>T (p.Thr205=) rs587780852 0.00002
NM_001148.6(ANK2):c.2796+15G>A rs371943204 0.00001
NM_001148.6(ANK2):c.3882C>T (p.Asn1294=) rs780187690 0.00001
NM_001148.6(ANK2):c.4372-20T>C rs748202207 0.00001
NM_001148.6(ANK2):c.10976G>T (p.Arg3659Leu) rs556640912
NM_001148.6(ANK2):c.11032+17G>A rs587780853
NM_001148.6(ANK2):c.1338T>A (p.Ile446=) rs1269042411
NM_001148.6(ANK2):c.2806C>G (p.Leu936Val) rs786205725
NM_001148.6(ANK2):c.3379+4C>A rs752152002

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