RS141542003 TMEM126B
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What This Variant Does
"Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype
Associated Conditions
Mitochondrial disease
Mitochondrial complex I deficiency
nuclear type 29
Mitochondrial disease
Mitochondrial complex I deficiency
nuclear type 29
Other Variants in TMEM126B