RS137852699 PPT1

Health Risk Chr 1:40097210
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What This Variant Does
"[OMIM:?]
Associated Conditions
Neuronal ceroid lipofuscinosis 1
Inborn genetic diseases
Neuronal ceroid lipofuscinosis
Neuronal ceroid lipofuscinosis 1
Inborn genetic diseases
Neuronal ceroid lipofuscinosis
Other Variants in PPT1
rs137852695 rs137852696 rs137852697 rs137852698 rs137852700 rs137852701 rs137852702 rs386833624 rs386833626 rs386833625
Ask Dr. Hemsworth about this variant