RS606231189 PDHA1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Pyruvate dehydrogenase E1-alpha deficiency
Inborn genetic diseases
Pyruvate dehydrogenase complex deficiency
Pyruvate dehydrogenase E1-alpha deficiency
Inborn genetic diseases
Pyruvate dehydrogenase complex deficiency
Other Variants in PDHA1