Gene entry
MT-CO3
No public annotation
- Chromosome
- —
- Cytoband
- —
- Variants (rsID)
- 55
MT-CO3 is a gene identifier without a current public annotation, located with no chromosome location recorded. The reference table lists 55 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs200809063Benignsingle nucleotide variantLeigh syndrome
- rs267606611Benignsingle nucleotide variantLeber optic atrophy|Leigh syndrome
- rs370688668Benignsingle nucleotide variant
- rs200613617Conflicting interpretationssingle nucleotide variantLeber optic atrophy|Leigh syndrome|See cases
- rs386829076Likely benignsingle nucleotide variant
Other listed variants
- rs2853826
- rs2854139
- rs2856985
- rs3134801
- rs3899188
- rs28358274
- rs28358276
- rs28358277
- rs28358278
- rs28358279
- rs28409867
- rs28411821
- rs28435660
- rs28457866
- rs28673954
- rs28715301
- rs28719882
- rs28754574
- rs41345446
- rs41347846
- rs41467651
- rs41487950
- rs121434456
- rs121434475
- rs121434476
- rs193302928
- rs199476117
- rs199476137
- rs199999390
- rs200048690
- rs200478835
- rs201397417
- rs201906571
- rs202131419
- rs267606890
- rs267606891
- rs369647419
- rs375959635
- rs376426900
- rs377413998
- rs377610479
- rs386829090
- rs386829092
- rs386829095
- rs387906731
- rs869082930
- rs878874133
- rs878916424
- rs879111957
- rs879214025
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.