RS886037835 TMEM126B
Upload your DNA to see your genotype for this variant.
What This Variant Does
"Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype
Associated Conditions
Mitochondrial complex I deficiency
nuclear type 29
Mitochondrial disease
Mitochondrial complex I deficiency
nuclear type 29
Mitochondrial disease
Other Variants in TMEM126B