Variant (rsID / SNP)
rs1042630
rs1042630 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACAN. Location: chromosome 15, position 89,402,051. The table records no clinical significance for this variant.
Reference-table entries
ACANNot classified
- Variant type
- missense_variant
- Chromosome / position
- 15:89402051
- HGVS
- NM_001369268.1,c.6235A>G,p.Ile2079Val
- Allele change
- Missense_I2079V
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.