RS200105202 AARS2

Health Risk Chr 6:44311148
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What This Variant Does
"CLNSIG=5
Associated Conditions
Combined oxidative phosphorylation defect type 8
Generalized muscle weakness
Leukoencephalopathy
progressive
with ovarian failure
Inborn genetic diseases
Cardiovascular phenotype
Combined oxidative phosphorylation defect type 8
Generalized muscle weakness
Leukoencephalopathy
progressive
with ovarian failure
Inborn genetic diseases
Cardiovascular phenotype
Other Variants in AARS2
rs138119149 rs387907061 rs78410483 rs587777589 rs587777590 rs587777591 rs146924860 rs747312867 rs200781477 rs863223859
Ask Dr. Hemsworth about this variant