RS118203992 TRMU
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What This Variant Does
"[OMIM:?]
Associated Conditions
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
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
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Aminoglycoside-induced deafness
Other Variants in TRMU