RS151344514 AFG3L2

Health Risk Chr 18:12337520
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Spinocerebellar ataxia type 28
Optic atrophy 12
Spastic ataxia 5
Spinocerebellar ataxia type 28
Optic atrophy 12
Spastic ataxia 5
Other Variants in AFG3L2
rs151344520 rs151344519 rs151344521 rs151344523 rs151344512 rs151344515 rs151344517 rs387906889 rs151344513 rs151344518
Ask Dr. Hemsworth about this variant