RS202189057 TPP1

Health Risk Chr 11:6617695
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Neuronal ceroid lipofuscinosis 2
Autosomal recessive spinocerebellar ataxia 7
Neuronal ceroid lipofuscinosis
Inborn genetic diseases
Neuronal ceroid lipofuscinosis 2
Autosomal recessive spinocerebellar ataxia 7
Neuronal ceroid lipofuscinosis
Other Variants in TPP1
rs119455953 rs119455954 rs119455955 rs56144125 rs119455956 rs28940573 rs119455957 rs119455958 rs755445790 rs121908197
Ask Dr. Hemsworth about this variant