RS139301835 SERAC1
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What This Variant Does
"CLNSIG=4
Associated Conditions
3-methylglutaconic aciduria with deafness
encephalopathy
and Leigh-like syndrome
Inborn genetic diseases
Mitochondrial oxidative phosphorylation disorder
3-methylglutaconic aciduria with deafness
encephalopathy
and Leigh-like syndrome
Inborn genetic diseases
Mitochondrial oxidative phosphorylation disorder
Other Variants in SERAC1