Variant (rsID / SNP)
rs11078234
rs11078234 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COX10. Location: chromosome 17, position 14,110,901. Clinical significance in the table: Benign.
Reference-table entries
COX10Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:14110901
- Cytoband
- 17p12
- HGVS
- NM_001303.4(COX10):c.*371A>G
- Allele change
- Silent
Associated conditions / phenotypes
Cytochrome-c oxidase deficiency disease|Leigh syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.