RS387907070 TMEM70

Health Risk Chr 8:73978783
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What This Variant Does
"CLNSIG=5
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 rs113669789 rs796052054 rs770816150 rs796052056 rs200820631 rs199655842 rs796052055 rs149823637
Ask Dr. Hemsworth about this variant