List of variants in gene PRPH2 reported as benign for Pigmentary retinal dystrophy

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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: 17

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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

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