RS201544686 MTO1

Health Risk Chr 6:73482209
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
Inborn genetic diseases
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
Inborn genetic diseases
Other Variants in MTO1
rs397518449 rs143747297 rs141970072 rs398122419 rs1060499776 rs746382157 rs748152539 rs1064793196 rs1025884753 rs200583827
Ask Dr. Hemsworth about this variant