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Variant (rsID / SNP)

rs1042631

ACAN

rs1042631 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACAN. Location: chromosome 15, position 89,402,239. The table records no clinical significance for this variant.

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Reference-table entries

ACANNot classified
Variant type
synonymous_variant
Chromosome / position
15:89402239
HGVS
NM_001369268.1,c.6423T>C,p.Leu2141Leu
Allele change
Synonymous_L2141L

Associated conditions / phenotypes

Degenerative Disc Disease

Public references

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