List of variants in gene PRPH2 reported as likely benign for Cone-rod 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000322.5(PRPH2):c.708C>T (p.Tyr236=)	rs61755813	0.00062
NM_000322.5(PRPH2):c.938C>T (p.Pro313Leu)	rs61748434	0.00044
NM_000322.5(PRPH2):c.*20C>T	rs180775924	0.00042
NM_000322.5(PRPH2):c.*1079G>A	rs572613522	0.00010
NM_000322.5(PRPH2):c.1008C>T (p.Gly336=)	rs752365478	0.00006
NM_000322.5(PRPH2):c.312C>T (p.Ile104=)	rs200009675	0.00004
NM_000322.5(PRPH2):c.454A>G (p.Met152Val)	rs146703538	0.00002
NM_000322.5(PRPH2):c.955T>C (p.Phe319Leu)	rs139329966	0.00002

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