List of variants in gene PRPF6 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_012469.4(PRPF6):c.*1T>C	rs1167495795
NM_012469.4(PRPF6):c.514C>T (p.Arg172Trp)	rs369787039
NM_012469.4(PRPF6):c.550G>C (p.Asp184His)	rs527236096

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