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Variant (rsID / SNP)

rs3817428

ACAN

rs3817428 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACAN. Location: chromosome 15, position 89,415,247. The table records no clinical significance for this variant.

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Reference-table entries

ACANNot classified
Variant type
missense_variant
Chromosome / position
15:89415247
HGVS
NM_001369268.1,c.7233C>G,p.Asp2411Glu
Allele change
Missense_D2335E

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.