RS868732642 MFSD8

Health Risk Chr 4:127938782
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Associated Conditions
Inborn genetic diseases
Neuronal ceroid lipofuscinosis 7
Retinal dystrophy
Hereditary ataxia
Late-infantile neuronal ceroid lipofuscinosis
Neuronal ceroid lipofuscinosis 7
Macular dystrophy with central cone involvement
Inborn genetic diseases
Neuronal ceroid lipofuscinosis 7
Retinal dystrophy
Hereditary ataxia
Late-infantile neuronal ceroid lipofuscinosis
Neuronal ceroid lipofuscinosis 7
Macular dystrophy with central cone involvement
Other Variants in MFSD8
rs118203975 rs118203976 rs118203977 rs118203978 rs267607235 rs140948465 rs1740291234 rs587778809 rs138072045 rs75039907
Ask Dr. Hemsworth about this variant