List of variants in gene combination LOC126860392, RP1 reported as benign for retinitis pigmentosa 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_006269.2(RP1):c.5071T>C (p.Ser1691Pro)	rs414352	0.25064
NM_006269.2(RP1):c.5008G>A (p.Ala1670Thr)	rs446227	0.21425
NM_006269.2(RP1):c.5175A>G (p.Gln1725=)	rs441800	0.20759

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