RS3038807 RTN2

Health Risk Chr 19:45496963
Upload your DNA to see your genotype for this variant.
Associated Conditions
Hereditary spastic paraplegia
Hereditary spastic paraplegia
Hereditary spastic paraplegia
Hereditary spastic paraplegia
Other Variants in RTN2
rs763387041 rs145653668 rs768449676 rs761286207 rs748397131 rs1568625691 rs1568624823 rs201387324 rs745409162 rs201863499
Ask Dr. Hemsworth about this variant