List of variants in gene WDR19 reported as likely 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
NM_025132.4(WDR19):c.3533G>A (p.Arg1178Gln)	rs79436363	0.00015
NM_025132.4(WDR19):c.641T>A (p.Leu214Ter)	rs751290509	0.00004
NM_025132.4(WDR19):c.2777G>T (p.Ser926Ile)	rs751386429

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