RS970768801 PDE6B

Health Risk Chr 4:625888
Upload your DNA to see your genotype for this variant.
Associated Conditions
Retinitis pigmentosa 40
Congenital stationary night blindness autosomal dominant 2
Retinitis pigmentosa 40
Congenital stationary night blindness autosomal dominant 2
Other Variants in PDE6B
rs121918579 rs121918580 rs730880317 rs121918581 rs121918582 rs1553801591 rs121918583 rs398123298 rs398123299 rs149293844
Ask Dr. Hemsworth about this variant