List of variants in gene DIAPH3 reported as pathogenic for perceptual disorders

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
NC_000013.11:g.60163938C>T	rs2138511736
NC_000013.11:g.60163939G>A	rs2138511749
NM_001042517.2(DIAPH3):c.2059del (p.Cys687fs)	rs2050261564

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