ClinVar Miner

List of variants in gene PRPH2 reported as likely benign by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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_000322.5(PRPH2):c.866C>T (p.Ser289Leu)	rs62645939	0.00079
NM_000322.5(PRPH2):c.249C>T (p.Tyr83=)	rs61755775	0.00053

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