RS1023544297 GFM1

Health Risk Chr 3:158658956
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Associated Conditions
Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
Inborn genetic diseases
Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
Inborn genetic diseases
Other Variants in GFM1
rs119470018 rs119470019 rs119470020 rs139430866 rs377352238 rs863224030 rs201304690 rs863224033 rs191462023 rs774456344
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