RS376562033 TSFM
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3
Nephrotic syndrome
type 21
Inborn genetic diseases
Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3
Nephrotic syndrome
type 21
Other Variants in TSFM