RS371526758 NMNAT1

Health Risk Chr 1:9982368
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What This Variant Does
"CLNSIG=5
Associated Conditions
Leber congenital amaurosis 9
Inborn genetic diseases
NMNAT1-related disorder
Leber congenital amaurosis 9
Inborn genetic diseases
NMNAT1-related disorder
Other Variants in NMNAT1
rs387907290 rs142968179 rs150726175 rs387907291 rs368062092 rs387907293 rs387907294 rs748902766 rs138613460 rs768528387
Ask Dr. Hemsworth about this variant