RS2140418135 TSFM

Health Risk Chr 12:57787146
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Associated Conditions
Inborn genetic diseases
Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3
Inborn genetic diseases
Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3
Other Variants in TSFM
rs121909485 rs368313488 rs138461986 rs201754030 rs587777688 rs587777689 rs863224936 rs138534976 rs144109380 rs183575246
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