List of variants in gene PRPH2 reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000322.5(PRPH2):c.909C>T (p.Ser303=)	rs144111167	0.00049
NM_000322.5(PRPH2):c.264A>C (p.Pro88=)	rs1294407459	0.00034
NM_000322.5(PRPH2):c.37C>T (p.Arg13Trp)	rs61754402	0.00018
NM_000322.5(PRPH2):c.300G>A (p.Pro100=)	rs150695654	0.00011
NM_000322.5(PRPH2):c.205G>T (p.Val69Leu)	rs558060514	0.00001

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