RS755445790 TPP1

Health Risk Chr 11:6616513
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Neuronal ceroid lipofuscinosis 2
Autosomal recessive spinocerebellar ataxia 7
Neuronal ceroid lipofuscinosis 2
Autosomal recessive spinocerebellar ataxia 7
Other Variants in TPP1
rs119455953 rs119455954 rs119455955 rs56144125 rs119455956 rs28940573 rs119455957 rs119455958 rs121908197 rs121908198
Ask Dr. Hemsworth about this variant