"Revvity Omics, Revvity"[submitter] AND "WNK1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1325363	NM_018979.4(WNK1):c.2374-2A>G	WNK1	Single nucleotide variant (intron variant +1 more)	not provided	GLikely pathogenic
Select item 2690454	NM_018979.4(WNK1):c.2692A>T (p.Thr898Ser)	WNK1 (T898S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 575636	NM_018979.4(WNK1):c.4703A>C (p.His1568Pro)	WNK1 (H1568P +3 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +2 more	GUncertain significance
Select item 2438607	NM_018979.4(WNK1):c.4882C>T (p.Pro1628Ser)	WNK1 (P1381S +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2690453	NM_018979.4(WNK1):c.5725C>T (p.Pro1909Ser)	WNK1 (P1661S +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1753793	NM_018979.4(WNK1):c.5731G>A (p.Gly1911Ser)	WNK1 (G1663S +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

ClinVar