List of variants in gene PRF1 reported as likely benign by GeneDx

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_001083116.3(PRF1):c.462A>G (p.Ala154=)	rs116554195	0.01461
NM_001083116.3(PRF1):c.435G>A (p.Val145=)	rs115281140	0.01056
NM_001083116.3(PRF1):c.755A>G (p.Asn252Ser)	rs28933375	0.00674

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