Variant (rsID / SNP)

rs9858542

rs9858542 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BSN. Location: chromosome 3, position 49,701,983. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

BSNNot classified

Variant type: synonymous_variant
Chromosome / position: 3:49701983
HGVS: NM_003458.4,c.11736G>A,p.Thr3912Thr
Allele change: Synonymous_T3912T

Associated conditions / phenotypes

Inflammatory Bowel Disease|Multiple Sclerosis

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.