RS397514478 RNF170
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant sensory ataxia 1
Spastic paraplegia 85
autosomal recessive
Autosomal dominant sensory ataxia 1
Spastic paraplegia 85
autosomal recessive
Other Variants in RNF170