RS267607235 MFSD8
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neuronal ceroid lipofuscinosis 7
Neuronal ceroid lipofuscinosis
Inborn genetic diseases
Macular dystrophy with central cone involvement
Neuronal ceroid lipofuscinosis 7
Neuronal ceroid lipofuscinosis
Inborn genetic diseases
Macular dystrophy with central cone involvement
Other Variants in MFSD8