ClinVar Miner

List of variants in gene combination ANK2, LOC126807136 reported as uncertain significance by GeneDx

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_001148.6(ANK2):c.6228G>T (p.Lys2076Asn) rs144848998 0.00050
NM_001148.6(ANK2):c.5509G>A (p.Ala1837Thr) rs199527708 0.00023
NM_001148.6(ANK2):c.5651C>T (p.Ser1884Leu) rs150737736 0.00015
NM_001148.6(ANK2):c.5570T>A (p.Val1857Glu) rs141212932 0.00006
NM_001148.6(ANK2):c.6143A>G (p.Gln2048Arg) rs201628725 0.00006
NM_001148.6(ANK2):c.6170C>T (p.Pro2057Leu) rs146531225 0.00005
NM_001148.6(ANK2):c.5182C>T (p.Leu1728Phe) rs1396790291 0.00004
NM_001148.6(ANK2):c.5329G>C (p.Val1777Leu) rs886059014 0.00004
NM_001148.6(ANK2):c.5438T>C (p.Leu1813Pro) rs1554552296 0.00004
NM_001148.6(ANK2):c.5758G>A (p.Gly1920Arg) rs140189724 0.00004
NM_001148.6(ANK2):c.5575C>A (p.Pro1859Thr) rs781312863 0.00003
NM_001148.6(ANK2):c.5588C>T (p.Thr1863Met) rs536962908 0.00003
NM_001148.6(ANK2):c.6205C>T (p.Arg2069Cys) rs754572911 0.00003
NM_001148.6(ANK2):c.5515A>C (p.Thr1839Pro) rs763795429 0.00002
NM_001148.6(ANK2):c.5552C>T (p.Thr1851Ile) rs376085805 0.00001
NM_001148.6(ANK2):c.5606C>T (p.Ala1869Val) rs983680857 0.00001
NM_001148.6(ANK2):c.5744C>T (p.Pro1915Leu) rs1717005319 0.00001
NM_001148.6(ANK2):c.5750C>T (p.Ser1917Leu) rs200929000 0.00001
NM_001148.6(ANK2):c.5957A>G (p.Glu1986Gly) rs1455187261 0.00001
NM_001148.6(ANK2):c.6185C>G (p.Ala2062Gly) rs1194235291 0.00001
NM_001148.6(ANK2):c.5213G>C (p.Gly1738Ala) rs145546655
NM_001148.6(ANK2):c.5231C>A (p.Ala1744Asp) rs147706514
NM_001148.6(ANK2):c.5234C>G (p.Pro1745Arg) rs751038588
NM_001148.6(ANK2):c.5263T>A (p.Ser1755Thr) rs2505324743
NM_001148.6(ANK2):c.5281A>T (p.Thr1761Ser) rs1325692328
NM_001148.6(ANK2):c.5296A>G (p.Ile1766Val) rs2154019333
NM_001148.6(ANK2):c.5348G>A (p.Gly1783Asp)
NM_001148.6(ANK2):c.5387_5389dup (p.Asp1796_Val1797insAsp)
NM_001148.6(ANK2):c.5492C>T (p.Ser1831Phe) rs1259276813
NM_001148.6(ANK2):c.5498T>C (p.Leu1833Pro)
NM_001148.6(ANK2):c.5566C>T (p.Pro1856Ser) rs2505387846
NM_001148.6(ANK2):c.5571_5642del (p.Ala1861_Ser1884del) rs2095591008
NM_001148.6(ANK2):c.5665A>G (p.Arg1889Gly) rs2154020406
NM_001148.6(ANK2):c.5783T>C (p.Val1928Ala)
NM_001148.6(ANK2):c.5893C>T (p.Pro1965Ser) rs2095620859
NM_001148.6(ANK2):c.5927C>G (p.Ser1976Cys) rs1447972755
NM_001148.6(ANK2):c.5963T>C (p.Met1988Thr) rs2154021231
NM_001148.6(ANK2):c.5969T>C (p.Val1990Ala)

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