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Variant (rsID / SNP)

rs938608

ACAN

rs938608 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACAN. Location: chromosome 15, position 89,398,605. The table records no clinical significance for this variant.

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Reference-table entries

ACANNot classified
Variant type
missense_variant
Chromosome / position
15:89398605
HGVS
NM_001369268.1,c.2789G>T,p.Ser930Ile
Allele change
Missense_S930I

Public references

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