ClinVar Miner

List of variants in gene ANK2 reported as benign for Cardiovascular phenotype

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Total variants: 42
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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.8503C>T (p.Pro2835Ser) rs3733617 0.14405
NM_001148.6(ANK2):c.9648A>G (p.Glu3216=) rs10013743 0.12780
NM_001148.6(ANK2):c.2337C>T (p.Val779=) rs29341 0.03480
NM_001148.6(ANK2):c.3510A>G (p.Val1170=) rs35336373 0.02906
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.9996T>C (p.Ser3332=) rs145557320 0.00778
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.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.1401A>G (p.Ala467=) rs142159132 0.00269
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.8979A>G (p.Ile2993Met) rs112252825 0.00064
NM_001148.6(ANK2):c.130C>G (p.Leu44Val) rs145272651 0.00051
NM_001148.6(ANK2):c.741C>T (p.Asn247=) rs190102899 0.00023
NM_001148.6(ANK2):c.8388G>A (p.Pro2796=) rs369684289 0.00021
NM_001148.6(ANK2):c.6633C>T (p.Ala2211=) rs143516811 0.00018
NM_001148.6(ANK2):c.85-4G>A rs377576219 0.00013
NM_001148.6(ANK2):c.11230A>C (p.Thr3744Pro) rs372212045 0.00010
NM_001148.6(ANK2):c.962G>A (p.Arg321Gln) rs150226540 0.00010
NM_001148.6(ANK2):c.3507T>C (p.Gly1169=) rs200262333 0.00008
NM_001148.6(ANK2):c.10032A>G (p.Pro3344=) rs775667097 0.00005
NM_001148.6(ANK2):c.9172C>T (p.Arg3058Cys) rs188282049 0.00005
NM_001148.6(ANK2):c.9242A>T (p.Asp3081Val) rs962522673 0.00005
NM_001148.6(ANK2):c.6662G>A (p.Gly2221Glu) rs185384934 0.00003
NM_001148.6(ANK2):c.10646G>A (p.Arg3549His) rs768351547 0.00002
NM_001148.6(ANK2):c.8423A>G (p.Tyr2808Cys) rs545512501 0.00002
NM_001148.6(ANK2):c.10263C>T (p.Ala3421=) rs745900850 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.4905G>C (p.Gly1635=)
NM_001148.6(ANK2):c.9474G>T (p.Pro3158=) rs145111737

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