Variant (rsID / SNP)

rs3743398

rs3743398 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACAN. Location: chromosome 15, position 89,398,407. The table records no clinical significance for this variant.

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Reference-table entries

ACANNot classified

Variant type: missense_variant
Chromosome / position: 15:89398407
HGVS: NM_001369268.1,c.2591C>T,p.Pro864Leu
Allele change: Missense_P864L

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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