List of variants in gene PDE6A reported as benign for perceptual disorders

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_000440.3(PDE6A):c.*756T>C	rs4705388	0.65681
NM_000440.3(PDE6A):c.*608T>C	rs4705389	0.64714
NM_000440.3(PDE6A):c.*796A>G	rs4705387	0.64137
NM_000440.3(PDE6A):c.*1365G>A	rs888895	0.62508
NM_000440.3(PDE6A):c.*2009T>C	rs2005909	0.61189
NM_000440.3(PDE6A):c.*2110A>G	rs759816	0.59199
NM_000440.3(PDE6A):c.*2194G>A	rs30886	0.44908
NM_000440.3(PDE6A):c.*2336C>T	rs30885	0.44141
NM_000440.3(PDE6A):c.*2542G>A	rs30884	0.37685
NM_000440.3(PDE6A):c.1408-34A>G	rs2244836	0.31937
NM_000440.3(PDE6A):c.331A>C (p.Arg111=)	rs2277925	0.21963
NM_000440.3(PDE6A):c.465C>T (p.Asn155=)	rs2277926	0.18879
NM_000440.3(PDE6A):c.2337T>C (p.Phe779=)	rs17110644	0.05660
NM_000440.3(PDE6A):c.2424G>A (p.Glu808=)	rs10067462	0.04249
NM_000440.3(PDE6A):c.1791C>T (p.Phe597=)	rs61733360	0.03204
NM_000440.3(PDE6A):c.2400C>T (p.Asp800=)	rs4705390	0.03160
NM_000440.3(PDE6A):c.*2769A>C	rs78827133	0.02540
NM_000440.3(PDE6A):c.*2771G>C	rs17110632	0.02378
NM_000440.3(PDE6A):c.1171G>A (p.Val391Met)	rs61732059	0.01720
NM_000440.3(PDE6A):c.1017T>C (p.His339=)	rs61733364	0.01655
NM_000440.3(PDE6A):c.1963C>T (p.His655Tyr)	rs78775072	0.01647
NM_000440.3(PDE6A):c.84C>T (p.Tyr28=)	rs34230349	0.01488
NM_000440.3(PDE6A):c.*1720T>A	rs74869635	0.00595
NM_000440.3(PDE6A):c.1086G>A (p.Ala362=)	rs142259966	0.00445
NM_000440.3(PDE6A):c.878C>T (p.Pro293Leu)	rs114973968	0.00309
NM_000440.3(PDE6A):c.498G>A (p.Val166=)	rs138274547	0.00092
NM_000440.3(PDE6A):c.177A>G (p.Glu59=)	rs146550067	0.00050
NM_000440.3(PDE6A):c.1954C>T (p.Arg652Cys)	rs199748187	0.00014
NM_000440.3(PDE6A):c.1927-21C>G	rs75282782
NM_000440.3(PDE6A):c.934-27_934-26del	rs60750624

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