"PreventionGenetics, part of Exact Sciences"[submitter] AND "WNT4"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3050685	NM_030761.5(WNT4):c.1032C>T (p.Leu344=)	WNT4	Single nucleotide variant (synonymous variant)	WNT4-related disorder	GLikely benign
Select item 2043091	NM_030761.5(WNT4):c.801T>A (p.Asp267Glu)	WNT4 (D267E)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2628841	NM_030761.5(WNT4):c.667G>A (p.Ala223Thr)	WNT4 (A223T)	Single nucleotide variant (missense variant)	WNT4-related disorder	GUncertain significance
Select item 2848815	NM_030761.5(WNT4):c.540G>A (p.Ser180=)	WNT4	Single nucleotide variant (synonymous variant)	WNT4-related disorder +1 more	GBenign/Likely benign
Select item 2719209	NM_030761.5(WNT4):c.313+10G>T	WNT4	Single nucleotide variant (intron variant)	WNT4-related disorder +1 more	GLikely benign
Select item 2630822	NM_030761.5(WNT4):c.203G>A (p.Arg68His)	WNT4 (R68H)	Single nucleotide variant (missense variant)	WNT4-related disorder	GUncertain significance
Select item 3061199	NM_030761.5(WNT4):c.126G>C (p.Thr42=)	WNT4	Single nucleotide variant (synonymous variant)	WNT4-related disorder	GLikely benign
Select item 3029272	NM_030761.5(WNT4):c.-9_-8dup	WNT4	Duplication (5 prime UTR variant)	WNT4-related disorder	GLikely benign

ClinVar