RS191462023 GFM1

Health Risk Chr 3:158649090
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
Other Variants in GFM1
rs119470018 rs119470019 rs119470020 rs139430866 rs377352238 rs863224030 rs201304690 rs863224033 rs774456344 rs201685981
Ask Dr. Hemsworth about this variant