RS184469579 TRIT1

Health Risk Chr 1:39883470
Upload your DNA to see your genotype for this variant.
Associated Conditions
TRIT1 Deficiency
Combined oxidative phosphorylation deficiency 35
Inborn genetic diseases
TRIT1 Deficiency
Combined oxidative phosphorylation deficiency 35
Inborn genetic diseases
Other Variants in TRIT1
rs2124597984 rs183302003 rs2522431304 rs2522401762 rs1642122631 rs2522382789 rs1367142675 rs1331558743 rs370866302 rs756728965
Ask Dr. Hemsworth about this variant