RS863224148 PDHA1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Pyruvate dehydrogenase E1-alpha deficiency
Abnormality of the mitochondrion
Pyruvate dehydrogenase complex deficiency
Inborn genetic diseases
Pyruvate dehydrogenase E1-alpha deficiency
Abnormality of the mitochondrion
Pyruvate dehydrogenase complex deficiency
Other Variants in PDHA1