RS724159970 MFSD8
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Neuronal ceroid lipofuscinosis 7
Macular dystrophy with central cone involvement
Late-infantile neuronal ceroid lipofuscinosis
Inborn genetic diseases
Neuronal ceroid lipofuscinosis 7
Macular dystrophy with central cone involvement
Late-infantile neuronal ceroid lipofuscinosis
Inborn genetic diseases
Other Variants in MFSD8