Variant (rsID / SNP)

rs137853580

rs137853580 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL10RA. Location: chromosome 11, position 117,860,219. Clinical significance in the table: Pathogenic.

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Reference-table entries

IL10RAPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 11:117860219
Cytoband: 11q23.3
HGVS: NM_001558.4(IL10RA):c.251C>T (p.Thr84Ile)
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.