Variant (rsID / SNP)

rs17118

rs17118 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XYLB. Location: chromosome 3, position 38,404,472. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

XYLBNot classified

Variant type: missense_variant
Chromosome / position: 3:38404472
HGVS: NM_001349178.2,c.255C>A,p.Asp85Glu
Allele change: Missense_D85E

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.