Variant (rsID / SNP)

rs1143627

rs1143627 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL1B. Location: chromosome 2, position 113,594,387. Clinical significance in the table: risk factor.

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Reference-table entries

IL1BRisk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 2:113594387
Cytoband: 2q14.1
HGVS: NM_000576.2(IL1B):c.-118C>T

Associated conditions / phenotypes

Gastric cancer susceptibility after h. pylori infection

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.