Variant (rsID / SNP)
rs698621
rs698621 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACAN. Location: chromosome 15, position 89,402,596. The table records no clinical significance for this variant.
Reference-table entries
ACANNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 15:89402596
- HGVS
- NM_001369268.1,c.6780T>G,p.Ala2260Ala
- Allele change
- Synonymous_A2260A
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.