List of variants in gene PRPH2 reported as likely pathogenic for Pigmentary retinal dystrophy

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_000322.5(PRPH2):c.469G>A (p.Asp157Asn)	rs61755787
NM_000322.5(PRPH2):c.535T>G (p.Trp179Gly)	rs61755796
NM_000322.5(PRPH2):c.793dup (p.Met265fs)	rs1800110234

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