RS121909485 TSFM

Health Risk Chr 12:57796539
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What This Variant Does
"[OMIM:?]
Associated Conditions
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
Inborn genetic diseases
Other Variants in TSFM
rs368313488 rs138461986 rs201754030 rs587777688 rs587777689 rs863224936 rs138534976 rs144109380 rs183575246 rs147317818
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