RS622288 MSTO1

Health Risk Chr 1:155612848
Upload your DNA to see your genotype for this variant.
Associated Conditions
Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome
Inborn genetic diseases
Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome
Inborn genetic diseases
Other Variants in MSTO1
rs1235749181 rs1673545403 rs767313156 rs149058840 rs371544149 rs1674934230 rs781637955 rs1673617254 rs955399709 rs745944305
Ask Dr. Hemsworth about this variant