List of variants in gene PRPH2 reported as benign for PRPH2-related disorder

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

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000322.5(PRPH2):c.929G>A (p.Arg310Lys)	rs425876	0.92861
NM_000322.5(PRPH2):c.910C>G (p.Gln304Glu)	rs390659	0.78498
NM_000322.5(PRPH2):c.1013A>G (p.Asp338Gly)	rs434102	0.77412
NM_000322.5(PRPH2):c.318T>C (p.Val106=)	rs7764439	0.59853
NM_000322.5(PRPH2):c.133C>T (p.Leu45Phe)	rs61755770	0.00414
NM_000322.5(PRPH2):c.909C>T (p.Ser303=)	rs144111167	0.00049
NM_000322.5(PRPH2):c.483C>T (p.Ile161=)	rs76989855
NM_000322.5(PRPH2):c.909_910delinsTG (p.Gln304Glu)	rs1582759657

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