List of variants in gene WAC reported as pathogenic for Inborn genetic diseases

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_016628.5(WAC):c.263_266del (p.Glu88fs)	rs864321689
NM_016628.5(WAC):c.305dup (p.His102fs)	rs2491926757
NM_016628.5(WAC):c.374C>A (p.Ser125Ter)	rs864321692

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