ClinVar Miner

List of variants in gene WNK1 reported by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Total variants: 20
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HGVS dbSNP
NM_018979.4(WNK1):c.1074C>T (p.Thr358=) rs72648621
NM_018979.4(WNK1):c.1769A>G (p.Lys590Arg) rs780986326
NM_018979.4(WNK1):c.1994C>T (p.Thr665Ile) rs2286007
NM_018979.4(WNK1):c.2336C>T (p.Ala779Val) rs141428612
NM_018979.4(WNK1):c.2490G>A (p.Pro830=) rs79816263
NM_018979.4(WNK1):c.2532T>A (p.Ile844=) rs762491690
NM_018979.4(WNK1):c.258T>C (p.Cys86=) rs3168640
NM_018979.4(WNK1):c.2896G>A (p.Val966Met) rs886042915
NM_018979.4(WNK1):c.3209+3A>G rs886044182
NM_018979.4(WNK1):c.3210T>C (p.Ser1070=) rs72650717
NM_018979.4(WNK1):c.3578G>A (p.Ser1193Asn) rs72650720
NM_018979.4(WNK1):c.3582G>A (p.Glu1194=) rs72650721
NM_018979.4(WNK1):c.46C>T (p.Leu16=) rs1443431827
NM_018979.4(WNK1):c.5281-4G>A rs72650740
NM_018979.4(WNK1):c.5520C>T (p.Val1840=) rs1212431255
NM_018979.4(WNK1):c.5583+3A>G rs72650758
NM_018979.4(WNK1):c.5734A>C (p.Ile1912Leu) rs201995891
NM_018979.4(WNK1):c.6150T>C (p.Leu2050=) rs151331381
NM_018979.4(WNK1):c.6278G>A (p.Arg2093His) rs200315094
NM_018979.4(WNK1):c.6624C>A (p.Ser2208Arg) rs72650768

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