RS113669789 TMEM70

Health Risk Chr 8:73978750
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Associated Conditions
Mitochondrial complex V (ATP synthase) deficiency
nuclear type 2
Autosomal recessive disease
Mitochondrial complex V (ATP synthase) deficiency
nuclear type 2
Autosomal recessive disease
Other Variants in TMEM70
rs183973249 rs1586636643 rs387907070 rs796052054 rs770816150 rs796052056 rs200820631 rs199655842 rs796052055 rs149823637
Ask Dr. Hemsworth about this variant