List of variants in gene WNK1 reported as benign by Eurofins NTD LLC (GA)

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_018979.4(WNK1):c.258T>C (p.Cys86=)	rs3168640	0.97485
NM_018979.4(WNK1):c.1994C>T (p.Thr665Ile)	rs2286007	0.05498
NM_018979.4(WNK1):c.5583+3A>G	rs72650758	0.00270
NM_018979.4(WNK1):c.2490G>A (p.Pro830=)	rs79816263	0.00211
NM_018979.4(WNK1):c.3582G>A (p.Glu1194=)	rs72650721	0.00173
NM_018979.4(WNK1):c.6624C>A (p.Ser2208Arg)	rs72650768

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