List of variants in gene PRPH2 reported as benign for Retinitis pigmentosa

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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: 26

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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.*1375C>T	rs405043	0.77180
NM_000322.5(PRPH2):c.*1357C>T	rs405059	0.77171
NM_000322.5(PRPH2):c.*543G>A	rs432753	0.77168
NM_000322.5(PRPH2):c.*762C>T	rs1758213	0.77165
NM_000322.5(PRPH2):c.318T>C (p.Val106=)	rs7764439	0.59853
NM_000322.5(PRPH2):c.*13C>T	rs361524	0.27666
NM_000322.5(PRPH2):c.*145G>A	rs835	0.24219
NM_000322.5(PRPH2):c.*898C>A	rs3176988	0.22759
NM_000322.5(PRPH2):c.*1001C>A	rs45550933	0.22757
NM_000322.5(PRPH2):c.-11A>C	rs114062933	0.03391
NM_000322.5(PRPH2):c.*132C>T	rs77363417	0.02609
NM_000322.5(PRPH2):c.*174C>T	rs73426412	0.02603
NM_000322.5(PRPH2):c.*276G>C	rs76754927	0.02448
NM_000322.5(PRPH2):c.*839G>A	rs73426405	0.02142
NM_000322.5(PRPH2):c.*1230C>T	rs79663042	0.01163
NM_000322.5(PRPH2):c.*1534T>C	rs115252154	0.00821
NM_000322.5(PRPH2):c.*989G>A	rs142990052	0.00657
NM_000322.5(PRPH2):c.*1313G>A	rs115451690	0.00625
NM_000322.5(PRPH2):c.133C>T (p.Leu45Phe)	rs61755770	0.00414
NM_000322.5(PRPH2):c.*1524G>C	rs183409467	0.00247
NM_000322.5(PRPH2):c.909C>T (p.Ser303=)	rs144111167	0.00049
NM_000322.5(PRPH2):c.37C>T (p.Arg13Trp)	rs61754402	0.00018
NM_000322.5(PRPH2):c.44A>G (p.Lys15Arg)	rs555112175	0.00006

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