Variant (rsID / SNP)

rs77877576

rs77877576 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COX10. Location: chromosome 17, position 13,972,860. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

COX10Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:13972860
Cytoband: 17p12
HGVS: NM_001303.4(COX10):c.-63C>T
Allele change: Silent

Associated conditions / phenotypes

Leigh syndrome|Cytochrome-c oxidase deficiency disease

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.