Variant (rsID / SNP)
rs2351491
rs2351491 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACAN. Location: chromosome 15, position 89,398,105. The table records no clinical significance for this variant.
Reference-table entries
ACANNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 15:89398105
- HGVS
- NM_001369268.1,c.2289C>T,p.Pro763Pro
- Allele change
- Synonymous_P763P
Associated conditions / phenotypes
Spinal Disease|Back Pain
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.