List of variants in gene PDE6A reported as benign by Illumina Laboratory Services, Illumina

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: 19

Download table as spreadsheet

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.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.*1720T>A	rs74869635	0.00595
NM_000440.3(PDE6A):c.177A>G (p.Glu59=)	rs146550067	0.00050

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.