PDE6C Chromosome 10

Phosphodiesterase 6C
128 variants 128 Health Risk

Upload your DNA to see your personal genotypes for variants in PDE6C.

What This Gene Does
This gene encodes the alpha-prime subunit of cone phosphodiesterase, which is composed of a homodimer of two alpha-prime subunits and 3 smaller proteins of 11, 13, and 15 kDa. Mutations in this gene are associated with cone dystrophy type 4 (COD4). [provided by RefSeq, Mar 2010]
Gene Info
Gene Group
Phosphodiesterases
Locus Type
gene with protein product
Location
10q23.33
Ensembl
ENSG00000095464
Associated Conditions (9)
Achromatopsia
Cone dystrophy 4
Retinal dystrophy
PDE6C-related disorder
Inborn genetic diseases
Achromatopsia 5
Cone dystrophy
Abnormality of the eye
Isolated macular dystrophy
Key Variants
All Variants (128)
RSID Category Clinical Significance Conditions
RS1051926 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Achromatopsia
RS1064797148 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Retinal dystrophy, Achromatopsia
RS1131978 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Achromatopsia
RS138970846 Health Risk Conflicting classifications of pathogenicity Cone dystrophy 4, Achromatopsia, Cone dystrophy 4
RS139456217 Health Risk Conflicting classifications of pathogenicity Cone dystrophy 4, Achromatopsia, PDE6C-related disorder
RS139638257 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS139652451 Health Risk Conflicting classifications of pathogenicity Cone dystrophy 4, Achromatopsia, Cone dystrophy 4
RS140469169 Health Risk Conflicting classifications of pathogenicity PDE6C-related disorder, PDE6C-related disorder
RS140524715 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, PDE6C-related disorder
RS142876079 Health Risk Conflicting classifications of pathogenicity Cone dystrophy 4, Achromatopsia, Inborn genetic diseases
RS145591492 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Achromatopsia
RS145836229 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Achromatopsia
RS148661165 Health Risk Conflicting classifications of pathogenicity Cone dystrophy 4, Achromatopsia, Cone dystrophy 4
RS150112560 Health Risk Conflicting classifications of pathogenicity Cone dystrophy 4, Achromatopsia, PDE6C-related disorder
RS181296577 Health Risk Conflicting classifications of pathogenicity Cone dystrophy 4, Achromatopsia, Cone dystrophy 4
RS199559247 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Achromatopsia
RS199704992 Health Risk Conflicting classifications of pathogenicity Cone dystrophy 4, Achromatopsia, Cone dystrophy 4
RS199926911 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200939953 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Achromatopsia
RS200979646 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Achromatopsia
RS201309785 Health Risk Conflicting classifications of pathogenicity
RS201702907 Health Risk Conflicting classifications of pathogenicity Cone dystrophy 4, Achromatopsia, Cone dystrophy 4
RS201956926 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Achromatopsia
RS202031903 Health Risk Conflicting classifications of pathogenicity Cone dystrophy 4, Achromatopsia, Cone dystrophy 4
RS2058524276 Health Risk Conflicting classifications of pathogenicity Cone dystrophy 4, Achromatopsia, Cone dystrophy 4
RS2133878975 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Achromatopsia
RS368331638 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Achromatopsia
RS375235184 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Retinal dystrophy
RS375795507 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Retinal dystrophy
RS41290222 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Achromatopsia
RS45522236 Health Risk Conflicting classifications of pathogenicity Cone dystrophy 4, Achromatopsia, Cone dystrophy 4
RS530593118 Health Risk Conflicting classifications of pathogenicity
RS534132522 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS535191090 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, PDE6C-related disorder, Retinal dystrophy
RS545034158 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Achromatopsia
RS568930062 Health Risk Conflicting classifications of pathogenicity PDE6C-related disorder, PDE6C-related disorder
RS752478645 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Achromatopsia
RS752963712 Health Risk Conflicting classifications of pathogenicity Cone dystrophy 4, Cone dystrophy 4
RS762152984 Health Risk Conflicting classifications of pathogenicity Achromatopsia 5, Achromatopsia, Achromatopsia 5
RS762809900 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Achromatopsia
RS765202218 Health Risk Conflicting classifications of pathogenicity Cone dystrophy 4, Achromatopsia, Cone dystrophy 4
RS781649493 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Achromatopsia
RS786205462 Health Risk Conflicting classifications of pathogenicity
RS79487435 Health Risk Conflicting classifications of pathogenicity Cone dystrophy 4, Achromatopsia, Cone dystrophy 4
RS886047482 Health Risk Conflicting classifications of pathogenicity Achromatopsia, Cone dystrophy 4, Achromatopsia
RS1023522305 Health Risk Likely pathogenic Achromatopsia, Cone dystrophy 4, Achromatopsia
RS1057518244 Health Risk Likely pathogenic
RS1344288054 Health Risk Likely pathogenic
RS139251833 Health Risk Likely pathogenic
RS1403661741 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
1 2 3 Next »
Sign Up to Analyze Your DNA Log In