RS121918582 PDE6B

Health Risk Chr 4:653912
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital stationary night blindness autosomal dominant 2
Congenital stationary night blindness autosomal dominant 2
Other Variants in PDE6B
rs121918579 rs121918580 rs730880317 rs121918581 rs1553801591 rs121918583 rs398123298 rs398123299 rs149293844 rs62295357
Ask Dr. Hemsworth about this variant