RS139430866 GFM1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
Combined oxidative phosphorylation deficiency
See cases
Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
Combined oxidative phosphorylation deficiency
See cases
Other Variants in GFM1