"Genetic Services Laboratory, University of Chicago"[submitter] AND "W - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 437268	NM_015910.7(WDPCP):c.1813-27A>G	WDPCP	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 531816	NM_015910.7(WDPCP):c.1438G>A (p.Val480Ile)	WDPCP (V480I +2 more)	Single nucleotide variant (missense variant +1 more)	WDPCP-related disorder +4 more	GUncertain significance
Select item 437269	NM_015910.7(WDPCP):c.1357G>A (p.Gly453Ser)	WDPCP (G453S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2443300	NM_015910.7(WDPCP):c.1109T>G (p.Val370Gly)	WDPCP (V211G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 437270	NM_015910.7(WDPCP):c.1102C>T (p.Arg368Cys)	WDPCP (R368C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GUncertain significance
Select item 336770	NM_015910.7(WDPCP):c.83A>T (p.Asp28Val)	WDPCP (D28V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 193388	NM_015910.7(WDPCP):c.68C>A (p.Pro23Gln)	WDPCP (P23Q)	Single nucleotide variant (5 prime UTR variant +2 more)	not provided +3 more	GBenign/Likely benign

ClinVar