RS753039116 TRMU
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Aminoglycoside-induced deafness
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Aminoglycoside-induced deafness
Other Variants in TRMU