ClinVar Miner

List of variants in gene ANK2 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Gene type:
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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_001148.6(ANK2):c.9061G>A (p.Ala3021Thr) rs74348333 0.00465
NM_001148.6(ANK2):c.4745G>A (p.Arg1582Gln) rs138842207 0.00090
NM_001148.6(ANK2):c.11231C>A (p.Thr3744Asn) rs121912705 0.00077
NM_001148.6(ANK2):c.8979A>G (p.Ile2993Met) rs112252825 0.00064
NM_001148.6(ANK2):c.9046G>A (p.Glu3016Lys) rs149963885 0.00052
NM_001148.6(ANK2):c.231G>A (p.Val77=) rs149699185 0.00049
NM_001148.6(ANK2):c.10531C>T (p.Leu3511=) rs148462839 0.00022
NM_001148.6(ANK2):c.3963T>C (p.Ile1321=) rs72901936 0.00020
NM_001148.6(ANK2):c.270G>T (p.Val90=) rs376457094 0.00016
NM_001148.6(ANK2):c.4372-7C>T rs370720661 0.00014
NM_001148.6(ANK2):c.962G>A (p.Arg321Gln) rs150226540 0.00010
NM_001148.6(ANK2):c.10809T>A (p.Ile3603=) rs924379504 0.00004
NM_001148.6(ANK2):c.2900+5125C>G rs779697542 0.00002
NM_001148.6(ANK2):c.3045A>T (p.Ala1015=) rs1588357219 0.00001
NM_001148.6(ANK2):c.1326C>T (p.Gly442=) rs1586382649
NM_001148.6(ANK2):c.3471C>T (p.Ile1157=) rs1157298737
NM_001148.6(ANK2):c.9039A>C (p.Ser3013=)

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