RS768063881 C19orf12

Health Risk Chr 19:29702961
Upload your DNA to see your genotype for this variant.
Associated Conditions
Neurodegeneration with brain iron accumulation 4
Hereditary spastic paraplegia 43
Neurodegeneration with brain iron accumulation 4
Hereditary spastic paraplegia 43
Other Variants in C19orf12
rs515726204 rs397514477 rs515726205 rs146170087 rs387907173 rs376103979 rs398122409 rs200133991 rs797045423 rs201987973
Ask Dr. Hemsworth about this variant