ClinVar Miner

List of variants in gene ANK2 reported as not provided by Cardiovascular Biomedical Research Unit, Royal Brompton & Harefield NHS Foundation Trust

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_001148.6(ANK2):c.11218C>A (p.Leu3740Ile) rs35530544 0.01031
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.10901T>A (p.Val3634Asp) rs66785829 0.00200
NM_001148.6(ANK2):c.11716C>T (p.Arg3906Trp) rs121912706 0.00094
NM_001148.6(ANK2):c.4373A>G (p.Glu1458Gly) rs72544141 0.00085
NM_001148.6(ANK2):c.11231C>A (p.Thr3744Asn) rs121912705 0.00077
NM_001148.6(ANK2):c.4315G>T (p.Gly1439Cys) rs34591340 0.00023
NM_001148.6(ANK2):c.11683G>A (p.Val3895Met) rs72556370 0.00007
NM_001148.6(ANK2):c.1423G>A (p.Gly475Arg) rs36210415 0.00006
NM_001148.6(ANK2):c.10708G>A (p.Glu3570Lys) rs180843436 0.00005
NM_001148.6(ANK2):c.11516G>C (p.Ser3839Thr) rs148654834 0.00004
NM_001148.6(ANK2):c.10900G>A (p.Val3634Ile) rs143228029 0.00002
NM_001148.6(ANK2):c.10858T>A (p.Trp3620Arg) rs199473346 0.00001
NM_001148.6(ANK2):c.11531C>A (p.Thr3844Asn) rs199473643 0.00001
NM_001148.6(ANK2):c.11086G>A (p.Glu3696Lys) rs199473347
NM_001148.6(ANK2):c.2122G>A (p.Val708Met) rs36210416
NM_001148.6(ANK2):c.4963C>A (p.Leu1655Met) rs199473343

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