RS61749755 GUCY2D

Health Risk Chr 17:8009531
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What This Variant Does
"[OMIM:?]
Associated Conditions
Leber congenital amaurosis 1
GUCY2D-related recessive retinopathy
Leber congenital amaurosis 1
GUCY2D-related recessive retinopathy
Other Variants in GUCY2D
rs61750172 rs61750173 rs267606857 rs386834239 rs61749676 rs61749679 rs61749682 rs61749683 rs63749078 rs61749758
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