"PreventionGenetics, part of Exact Sciences"[submitter] AND "WDR73"[ge - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 286528	NM_032856.5(WDR73):c.1132dup (p.Arg378fs)	WDR73 (R378fs)	Duplication (frameshift variant +1 more)	WDR73-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 786630	NM_032856.5(WDR73):c.1126G>T (p.Ala376Ser)	WDR73 (A376S)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 3043644	NM_032856.5(WDR73):c.1038C>T (p.Thr346=)	WDR73	Single nucleotide variant (synonymous variant +1 more)	WDR73-related disorder	GLikely benign
Select item 718589	NM_032856.5(WDR73):c.1011G>T (p.Gly337=)	WDR73	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 500421	NM_032856.5(WDR73):c.935G>A (p.Arg312Gln)	WDR73 (R312Q)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 785506	NM_032856.5(WDR73):c.928G>A (p.Gly310Arg)	WDR73 (G310R)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 225244	NM_032856.5(WDR73):c.888del (p.Phe296fs)	WDR73 (F296fs)	Deletion (frameshift variant +1 more)	Galloway-Mowat syndrome 1 +2 more	GPathogenic
Select item 3054147	NM_032856.5(WDR73):c.828A>G (p.Pro276=)	WDR73	Single nucleotide variant (synonymous variant +1 more)	WDR73-related disorder	GLikely benign
Select item 2170134	NM_032856.5(WDR73):c.732T>G (p.Leu244=)	WDR73	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3032410	NM_032856.5(WDR73):c.714G>C (p.Gly238=)	WDR73	Single nucleotide variant (synonymous variant +1 more)	WDR73-related disorder	GLikely benign
Select item 2182122	NM_032856.5(WDR73):c.507G>A (p.Thr169=)	WDR73	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 729194	NM_032856.5(WDR73):c.480C>T (p.Val160=)	WDR73	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2150651	NM_032856.5(WDR73):c.288-6dup	WDR73	Duplication (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 728212	NM_032856.5(WDR73):c.267A>G (p.Leu89=)	WDR73	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GLikely benign