Variant (rsID / SNP)

rs2281636

rs2281636 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COX15. Location: chromosome 10, position 101,492,403. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

COX15Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:101492403
Cytoband: 10q24.2
HGVS: NM_015960.3(CUTC):c.61+237T>G
Allele change: Silent

Associated conditions / phenotypes

Leigh syndrome

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.