List of variants in gene PRPF4 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001244926.2(PRPF4):c.941C>T (p.Pro314Leu)	rs587777599	0.00001
NC_000009.12:g.113275630TGTCAGTGACGCACTTCC[1]	rs541873609

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