rs5498
This is a variant in the ICAM1 gene that changes a lysine to an glutamate.
▶GWAS Catalog Trait Associations (7)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (7)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
intercellular adhesion molecule 1 measurement
protein measurement
ICAM-1 measurement
intercellular adhesion molecule 5 measurement
neutrophil-to-lymphocyte ratio
diastolic blood pressure
lymphocyte count
▶ClinVar annotation
▶Research that mentions this SNP (2)
▶Genome‐wide association studies of cerebral white matter lesion burdenMeta-analysisN=12,385Fornage M. et al.(2011)· Annals of Neurology
Genome-wide meta-analysis of 9,361 Europeans identified six genome-wide significant SNPs on chromosome 17q25 associated with white matter hyperintensity (WMH) burden. The most significant SNP, rs3744028 (P = 4.0×10⁻⁹ discovery, P = 1.3×10⁻⁷ replication, P = 4.0×10⁻¹⁵ combined), and rs1055129 were replicated in 3,024 additional individuals. Risk alleles increased WMH burden by 4-8% of mean burden.
▶ICAM gene cluster SNPs and prostate cancer risk in African AmericansAssociationN=677Hankui Chen et al.(2006)· Human Genetics
A case-control study in African American men (286 cases, 391 controls) confirmed that ICAM1 SNPs -9A/C (rs5490, OR=2.5) and K469E (rs5498, OR=1.8) are associated with prostate cancer risk in familial disease. A common ICAM haplotype containing the -9A/C variant was significantly associated with prostate cancer (P=0.03), particularly in men with family history. Unlike previous findings in European populations, ICAM5 SNPs were not associated with prostate cancer in African Americans.
About ICAM1
This gene encodes a cell surface glycoprotein which is typically expressed on endothelial cells and cells of the immune system. It binds to integrins of type CD11a / CD18, or CD11b / CD18 and is also exploited by Rhinovirus as a receptor. [provided by RefSeq, Jul 2008]
View all ICAM1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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