RS761283105 GFM2

Health Risk Chr 5:74747731
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Mitochondrial disease
Combined oxidative phosphorylation deficiency 39
Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
Mitochondrial disease
Combined oxidative phosphorylation deficiency 39
Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
Other Variants in GFM2
rs2478868062 rs139901493 rs924438731 rs752145775 rs757683184 rs751099539 rs1370043372 rs764127754 rs543482000 rs143233751
Ask Dr. Hemsworth about this variant