ClinVar Miner

List of variants in gene WNK1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_018979.4(WNK1):c.5583+3A>G rs72650758 0.00270
NM_018979.4(WNK1):c.5281-4G>A rs72650740 0.00269
NM_213655.5(WNK1):c.2172T>C (p.Val724=) rs72649808 0.00266
NM_018979.4(WNK1):c.2490G>A (p.Pro830=) rs79816263 0.00211
NM_213655.5(WNK1):c.2362C>T (p.Arg788Cys) rs72649848 0.00173
NM_018979.4(WNK1):c.1074C>T (p.Thr358=) rs72648621 0.00160
NM_018979.4(WNK1):c.6150T>C (p.Leu2050=) rs151331381 0.00157
NM_018979.4(WNK1):c.5284C>T (p.Leu1762=) rs72650741 0.00116
NM_018979.4(WNK1):c.1855A>G (p.Thr619Ala) rs149388376 0.00086
NM_018979.4(WNK1):c.4983T>C (p.Ser1661=) rs149852592 0.00072
NM_018979.4(WNK1):c.4354A>G (p.Thr1452Ala) rs142543401 0.00061
NM_018979.4(WNK1):c.915G>A (p.Thr305=) rs72648609 0.00048
NM_018979.4(WNK1):c.1044C>T (p.Arg348=) rs201400797 0.00014
NM_018979.4(WNK1):c.210G>A (p.Ala70=) rs145076179 0.00011
NM_018979.4(WNK1):c.2652G>A (p.Ala884=) rs142528714 0.00006
NM_018979.4(WNK1):c.6030G>A (p.Pro2010=) rs777053734 0.00004
NM_018979.4(WNK1):c.3906T>C (p.Ser1302=) rs1318518629 0.00002
NM_018979.4(WNK1):c.5325C>T (p.Ser1775=) rs373370309 0.00002
NM_018979.4(WNK1):c.2262A>C (p.Thr754=)
NM_018979.4(WNK1):c.2430G>A (p.Ala810=) rs201913428
NM_018979.4(WNK1):c.4354A>C (p.Thr1452Pro)
NM_018979.4(WNK1):c.4605_4607del (p.Ser1536del) rs72650732
NM_018979.4(WNK1):c.4968A>G (p.Glu1656=)
NM_018979.4(WNK1):c.5542_5550del (p.Thr1848_Ser1850del) rs544395150

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