Gene entry
MT-ATP6
No public annotation
- Chromosome
- —
- Cytoband
- —
- Variants (rsID)
- 118
MT-ATP6 is a gene identifier without a current public annotation, located with no chromosome location recorded. The reference table lists 118 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs199476137Likely pathogenicDeletionSeizures and lactic acidosis|Leber optic atrophy|Mitochondrial disease
- rs387906422Likely pathogenicsingle nucleotide variantCardiomyopathy, infantile hypertrophic|Histiocytoid cardiomyopathy|Mitochondrial disease
- rs199476138Pathogenicsingle nucleotide variantLeigh syndrome|Charcot-Marie-Tooth disease|Mitochondrial disease|Mitochondrial complex 5 (ATP synthase) deficiency, mitochondrial type 1|Leber optic atrophy|Mitochondrial DNA-Associated Leigh Syndrome and NARP
Other listed variants
- rs1064597
- rs1116904
- rs1116906
- rs1970771
- rs1978028
- rs1981459
- rs2248727
- rs2298009
- rs2298011
- rs2853818
- rs2853824
- rs2853825
- rs3020563
- rs3135028
- rs3929989
- rs9783079
- rs28358270
- rs28358272
- rs28358870
- rs28358872
- rs28358874
- rs28358879
- rs28358883
- rs28358884
- rs28380140
- rs28410416
- rs28415137
- rs28449754
- rs28451817
- rs28461343
- rs28474779
- rs28575684
- rs28637353
- rs28651339
- rs28660616
- rs28679680
- rs28705169
- rs41352249
- rs41413745
- rs41432347
- rs41482146
- rs41513156
- rs56041322
- rs121434454
- rs193303052
- rs199476127
- rs199616772
- rs200784106
- rs200811540
- rs201336180
- rs201559119
- rs201902227
- rs201950015
- rs267606611
- rs267606881
- rs367578507
- rs368623956
- rs369661971
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.