List of variants in gene combination LOC126860392, RP1 reported as likely benign for retinal disorder

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_006269.2(RP1):c.5701C>T (p.Leu1901Phe)	rs113793810	0.00389
NM_006269.2(RP1):c.6064A>C (p.Lys2022Gln)	rs184596875	0.00121
NM_006269.2(RP1):c.5624G>C (p.Gly1875Ala)	rs150728667	0.00054
NM_006269.2(RP1):c.5335A>T (p.Asn1779Tyr)	rs748293359	0.00006
NM_006269.2(RP1):c.5913C>A (p.Asn1971Lys)	rs754290174	0.00001
NM_006269.2(RP1):c.5552A>C (p.His1851Pro)

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