List of variants in gene RPGR reported as likely benign for X-linked cone-rod dystrophy 1

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001034853.2(RPGR):c.2057T>A (p.Met686Lys)	rs151247357	0.00794
NM_001034853.2(RPGR):c.2793G>A (p.Glu931=)	rs1446705794	0.00203
NM_001034853.2(RPGR):c.1240G>C (p.Glu414Gln)	rs150549982	0.00046
NM_001034853.2(RPGR):c.1708A>G (p.Thr570Ala)	rs768169831	0.00012
NM_001034853.2(RPGR):c.1348T>C (p.Cys450Arg)	rs794727019	0.00001

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