List of variants in gene WDFY3 reported as pathogenic for Neurodevelopmental disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_014991.6(WDFY3):c.10117G>T (p.Glu3373Ter)
NM_014991.6(WDFY3):c.3547C>T (p.Arg1183Ter)	rs2533592177
NM_014991.6(WDFY3):c.3579G>A (p.Trp1193Ter)	rs2533590867

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