RS144042123 TRIT1

Health Risk Chr 1:39847247
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Associated Conditions
Combined oxidative phosphorylation deficiency 35
Inborn genetic diseases
TRIT1-related disorder
Combined oxidative phosphorylation deficiency 35
Inborn genetic diseases
TRIT1-related disorder
Other Variants in TRIT1
rs2124597984 rs183302003 rs2522431304 rs2522401762 rs1642122631 rs2522382789 rs1367142675 rs1331558743 rs370866302 rs756728965
Ask Dr. Hemsworth about this variant