RS115775983 PDE6B

Health Risk Chr 4:634703 snv stop gained
Upload your DNA to see your genotype for this variant.
Associated Conditions
Retinitis pigmentosa
Congenital stationary night blindness autosomal dominant 2
Retinal dystrophy
Retinitis pigmentosa
Congenital stationary night blindness autosomal dominant 2
Retinal dystrophy
Population Frequencies
gnomAD ALL
1.2%
1kG AFR
0.2%
1kG ALL
0.5%
1kG AMR
1%
1kG EAS
100%
1kG EUR
1.1%
1kG SAS
99.5%
Other Variants in PDE6B
rs121918579 rs121918580 rs730880317 rs121918581 rs121918582 rs1553801591 rs121918583 rs398123298 rs398123299 rs149293844
Ask Dr. Hemsworth about this variant