List of variants in gene WNK1 reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 45

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HGVS	dbSNP	gnomAD frequency
NM_018979.4(WNK1):c.3166A>C (p.Thr1056Pro)	rs956868	0.84165
NM_018979.4(WNK1):c.1994C>T (p.Thr665Ile)	rs2286007	0.05498
NM_018979.4(WNK1):c.3490-5T>A	rs72650719	0.01759
NM_018979.4(WNK1):c.1512A>G (p.Leu504=)	rs56325964	0.01671
NM_018979.4(WNK1):c.2081T>C (p.Ile694Thr)	rs61736905	0.01664
NM_018979.4(WNK1):c.1526T>C (p.Ile509Thr)	rs34728563	0.01649
NM_018979.4(WNK1):c.5468C>T (p.Pro1823Leu)	rs17755373	0.00870
NM_018979.4(WNK1):c.5991G>A (p.Glu1997=)	rs61736907	0.00815
NM_018979.4(WNK1):c.684C>T (p.Gly228=)	rs72647374	0.00748
NM_018979.4(WNK1):c.3654A>G (p.Ser1218=)	rs141971833	0.00316
NM_018979.4(WNK1):c.5583+3A>G	rs72650758	0.00270
NM_018979.4(WNK1):c.5281-4G>A	rs72650740	0.00269
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.3112-10C>T	rs72650715	0.00103
NM_018979.4(WNK1):c.6643+18A>G	rs72650769	0.00103
NM_018979.4(WNK1):c.446C>T (p.Ala149Val)	rs34880640	0.00091
NM_018979.4(WNK1):c.1855A>G (p.Thr619Ala)	rs149388376	0.00086
NM_018979.4(WNK1):c.2459C>G (p.Ser820Cys)	rs74056058	0.00074
NM_018979.4(WNK1):c.4983T>C (p.Ser1661=)	rs149852592	0.00072
NM_018979.4(WNK1):c.7021G>A (p.Gly2341Ser)	rs146042595	0.00062
NM_018979.4(WNK1):c.4354A>G (p.Thr1452Ala)	rs142543401	0.00061
NM_018979.4(WNK1):c.578C>A (p.Pro193Gln)	rs72647372	0.00058
NM_018979.4(WNK1):c.2401A>G (p.Ile801Val)	rs139449198	0.00053
NM_018979.4(WNK1):c.915G>A (p.Thr305=)	rs72648609	0.00048
NM_018979.4(WNK1):c.3578G>A (p.Ser1193Asn)	rs72650720	0.00045
NM_213655.5(WNK1):c.2939G>T (p.Ser980Ile)	rs372091476	0.00026
NM_213655.5(WNK1):c.3371G>A (p.Gly1124Glu)	rs201042606	0.00024
NM_018979.4(WNK1):c.5833C>T (p.Arg1945Cys)	rs117016551	0.00021
NM_018979.4(WNK1):c.1834G>A (p.Gly612Ser)	rs146450828	0.00014
NM_018979.4(WNK1):c.2664A>G (p.Val888=)	rs769020140	0.00012
NM_018979.4(WNK1):c.5418A>G (p.Pro1806=)	rs56245971	0.00009
NM_018979.4(WNK1):c.187A>C (p.Lys63Gln)	rs780699781	0.00004
NM_018979.4(WNK1):c.4265T>G (p.Val1422Gly)	rs779654189	0.00004
NM_018979.4(WNK1):c.5462C>T (p.Ala1821Val)	rs371264719	0.00004
NM_018979.4(WNK1):c.130G>A (p.Ala44Thr)	rs764240024	0.00003
NM_018979.4(WNK1):c.6021A>G (p.Leu2007=)	rs1466331283	0.00001
NM_213655.5(WNK1):c.3575C>T (p.Thr1192Ile)	rs1217942716	0.00001
NM_018979.4(WNK1):c.1767C>G (p.Leu589=)
NM_018979.4(WNK1):c.1776G>A (p.Gln592=)	rs747700724
NM_018979.4(WNK1):c.4605_4607del (p.Ser1536del)	rs72650732
NM_018979.4(WNK1):c.5542_5550del (p.Thr1848_Ser1850del)	rs544395150
NM_018979.4(WNK1):c.6574G>A (p.Asp2192Asn)	rs747750974

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