List of variants in gene PRPH2 reported as benign for not specified

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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: 10

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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.*13C>T	rs361524	0.27666
NM_000322.5(PRPH2):c.829-48C>T	rs41273820	0.22114
NM_000322.5(PRPH2):c.-11A>C	rs114062933	0.03391
NM_000322.5(PRPH2):c.249C>T (p.Tyr83=)	rs61755775	0.00053
NM_000322.5(PRPH2):c.409G>A (p.Gly137Ser)	rs781256236	0.00002
NM_000322.5(PRPH2):c.464C>G (p.Thr155Ser)	rs199572514

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