RS141772938 ACO2

Health Risk Chr 22:41507837
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Optic atrophy 9
Infantile cerebellar-retinal degeneration
OPTIC ATROPHY 9
AUTOSOMAL RECESSIVE
ACO2-related disorder
Retinal dystrophy
Optic atrophy
Optic atrophy 9
Infantile cerebellar-retinal degeneration
OPTIC ATROPHY 9
AUTOSOMAL RECESSIVE
ACO2-related disorder
Retinal dystrophy
Optic atrophy
Other Variants in ACO2
rs786200924 rs387907389 rs752034900 rs786204828 rs786204829 rs786204830 rs747330606 rs863223881 rs864309499 rs375761361
Ask Dr. Hemsworth about this variant