RS559155109 MFSD8

Health Risk Chr 4:127920826
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What This Variant Does
"CLNSIG=4
Associated Conditions
Severe early-childhood-onset retinal dystrophy
Retinal dystrophy
Retinitis pigmentosa
Neuronal ceroid lipofuscinosis 7
Macular dystrophy with central cone involvement
Neuronal ceroid lipofuscinosis
Inborn genetic diseases
Cone-rod dystrophy
Severe early-childhood-onset retinal dystrophy
Retinal dystrophy
Retinitis pigmentosa
Neuronal ceroid lipofuscinosis 7
Macular dystrophy with central cone involvement
Neuronal ceroid lipofuscinosis
Inborn genetic diseases
Other Variants in MFSD8
rs118203975 rs118203976 rs118203977 rs118203978 rs267607235 rs140948465 rs1740291234 rs587778809 rs138072045 rs75039907
Ask Dr. Hemsworth about this variant