List of variants in gene WNK1 reported as likely 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: 16

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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_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.4354A>G (p.Thr1452Ala)	rs142543401	0.00061
NM_018979.4(WNK1):c.915G>A (p.Thr305=)	rs72648609	0.00048
NM_018979.4(WNK1):c.5418A>G (p.Pro1806=)	rs56245971	0.00009
NM_018979.4(WNK1):c.6021A>G (p.Leu2007=)	rs1466331283	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

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