List of variants in gene WNK4 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_032387.5(WNK4):c.1477-13A>G	rs61754357	0.02638
NM_032387.5(WNK4):c.1719C>T (p.His573=)	rs56243382	0.01157
NM_032387.5(WNK4):c.2029C>T (p.Arg677Trp)	rs9896991	0.01047
NM_032387.5(WNK4):c.3432-20T>C	rs61755630	0.00241
NM_032387.5(WNK4):c.2157+6G>C	rs61755607	0.00077
NM_032387.5(WNK4):c.2207G>A (p.Arg736Gln)	rs149389156	0.00061
NM_032387.5(WNK4):c.1853G>T (p.Cys618Phe)	rs143396070	0.00043
NM_032387.5(WNK4):c.1864-11T>C	rs61755599	0.00041
NM_032387.5(WNK4):c.1572G>T (p.Leu524=)	rs144084546	0.00033
NM_032387.5(WNK4):c.47C>T (p.Thr16Ile)	rs61754325	0.00030
NM_032387.5(WNK4):c.2213G>A (p.Arg738Gln)	rs200823152	0.00026
NM_032387.5(WNK4):c.92C>A (p.Ala31Glu)	rs370527167	0.00014
NM_032387.5(WNK4):c.1827A>G (p.Pro609=)	rs201340788	0.00006
NM_032387.5(WNK4):c.1743G>A (p.Ser581=)	rs754495845	0.00004
NM_032387.5(WNK4):c.2136G>A (p.Pro712=)	rs372128794	0.00003
NM_032387.5(WNK4):c.1666C>A (p.Pro556Thr)	rs56003090
NM_032387.5(WNK4):c.1818G>A (p.Gly606=)	rs149633706
NM_032387.5(WNK4):c.204G>A (p.Gly68=)	rs200209645
NM_032387.5(WNK4):c.2310A>G (p.Pro770=)	rs1597903569

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