ClinVar Miner

List of variants in gene PRPH2 reported as likely benign for Retinal dystrophy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000322.5(PRPH2):c.938C>T (p.Pro313Leu)	rs61748434	0.00044
NM_000322.5(PRPH2):c.507C>T (p.Asn169=)	rs143096101	0.00013

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