RS118203990 TRMU

Health Risk Chr 22:46337925
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What This Variant Does
"[OMIM:?]
Associated Conditions
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Aminoglycoside-induced deafness
TRMU-related disorder
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Aminoglycoside-induced deafness
TRMU-related disorder
Other Variants in TRMU
rs118203991 rs118203992 rs387907022 rs113846383 rs773023974 rs55952751 rs367570778 rs863224239 rs367683258 rs863224241
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