"Genome-Nilou Lab"[submitter] AND "WDR35"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 333371	NM_020779.4(WDR35):c.3121+12A>C	WDR35	Single nucleotide variant (intron variant)	Short-rib thoracic dysplasia 7 with or without polydactyly +3 more	GBenign
Select item 167844	NM_020779.4(WDR35):c.2915A>G (p.Glu972Gly)	WDR35 (E983G +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign
Select item 167846	NM_020779.4(WDR35):c.2824-14G>T	WDR35	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 256877	NM_020779.4(WDR35):c.2496A>G (p.Glu832=)	WDR35	Single nucleotide variant (synonymous variant)	Short-rib thoracic dysplasia 7 with or without polydactyly +3 more	GBenign
Select item 333407	NM_020779.4(WDR35):c.53A>G (p.Gln18Arg)	WDR35, MATN3 (Q18R)	Single nucleotide variant (missense variant)	Short-rib thoracic dysplasia 7 with or without polydactyly +6 more	GBenign/Likely benign
Select item 256876	NM_020779.4(WDR35):c.25-46G>A	WDR35	Single nucleotide variant (intron variant)	not provided +3 more	GBenign

ClinVar