List of variants in gene WNK1 reported as benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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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.446C>T (p.Ala149Val)	rs34880640	0.00091
NM_018979.4(WNK1):c.4983T>C (p.Ser1661=)	rs149852592	0.00072
NM_018979.4(WNK1):c.2401A>G (p.Ile801Val)	rs139449198	0.00053
NM_018979.4(WNK1):c.2664A>G (p.Val888=)	rs769020140	0.00012

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