Variant (rsID / SNP)

rs3135932

rs3135932 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL10RA. Location: chromosome 11, position 117,864,063. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

IL10RABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:117864063
Cytoband: 11q23.3
HGVS: NM_001558.4(IL10RA):c.475A>G (p.Ser159Gly)
Allele change: Silent

Associated conditions / phenotypes

Inflammatory bowel disease 28

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.