RS145756948 PDE6B

Health Risk Chr 4:654153
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Associated Conditions
Congenital stationary night blindness autosomal dominant 2
Retinitis pigmentosa
Inborn genetic diseases
Congenital stationary night blindness autosomal dominant 2
Retinitis pigmentosa
Inborn genetic diseases
Other Variants in PDE6B
rs121918579 rs121918580 rs730880317 rs121918581 rs121918582 rs1553801591 rs121918583 rs398123298 rs398123299 rs149293844
Ask Dr. Hemsworth about this variant