RS1215450178 TMEM70

Health Risk Chr 8:73976305
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Associated Conditions
Mitochondrial complex V (ATP synthase) deficiency
nuclear type 2
Inborn genetic diseases
Mitochondrial complex V (ATP synthase) deficiency
nuclear type 2
Inborn genetic diseases
Other Variants in TMEM70
rs183973249 rs1586636643 rs387907070 rs113669789 rs796052054 rs770816150 rs796052056 rs200820631 rs199655842 rs796052055
Ask Dr. Hemsworth about this variant