RS764871960 MSTO1

Health Risk Chr 1:155612219
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Associated Conditions
Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome
Inborn genetic diseases
Congenital cerebellar hypoplasia
Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome
Inborn genetic diseases
Congenital cerebellar hypoplasia
Other Variants in MSTO1
rs1674934230 rs745944305 rs1673545403 rs767313156 rs149058840 rs371544149 rs781637955 rs1673617254 rs955399709 rs752022363
Ask Dr. Hemsworth about this variant