RS137852700 PPT1

Health Risk Chr 1:40089495
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What This Variant Does
"[OMIM:?]
Associated Conditions
Neuronal ceroid lipofuscinosis 1
Neuronal Ceroid-Lipofuscinosis
Recessive
Neuronal ceroid lipofuscinosis
Inborn genetic diseases
PPT1-related disorder
Neuronal ceroid lipofuscinosis 1
Neuronal Ceroid-Lipofuscinosis
Recessive
Neuronal ceroid lipofuscinosis
Inborn genetic diseases
PPT1-related disorder
Other Variants in PPT1
rs137852695 rs137852696 rs137852697 rs137852698 rs137852699 rs137852701 rs137852702 rs386833624 rs386833626 rs386833625
Ask Dr. Hemsworth about this variant