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rs1554286

From SNPedia

Orientationminus
Stabilizedminus
Make rs1554286(C;C)
Make rs1554286(C;T)
Make rs1554286(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position206770888
GeneIL10
is asnp
is mentioned by
dbSNPrs1554286
ebirs1554286
HLIrs1554286
Exacrs1554286
Varsomers1554286
Maprs1554286
PheGenIrs1554286
hapmaprs1554286
1000 genomesrs1554286
hgdprs1554286
ensemblrs1554286
gopubmedrs1554286
geneviewrs1554286
scholarrs1554286
googlers1554286
pharmgkbrs1554286
gwascentralrs1554286
openSNPrs1554286
23andMers1554286
23andMe allrs1554286
SNP Nexus

SNPshotrs1554286
SNPdbers1554286
MSV3drs1554286
GWAS Ctlgrs1554286
GMAF0.3811
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20804371] Association between Single-Nucleotide Polymorphisms in Mal/TIRAP and Interleukin-10 Genes and Susceptibility to Invasive Haemophilus influenzae Serotype b Infection in Immunized Children


[PMID 21917900] Genetic Variations and Interactions in Anti-inflammatory Cytokine Pathway Genes in the Outcome of Leprosy: A Study Conducted on a MassARRAY Platform

[PMID 16672419OA-icon.png] Polymorphisms in the genes encoding chemokine receptor 5, interleukin-10, and monocyte chemoattractant protein 1 contribute to cytomegalovirus reactivation and disease after allogeneic stem cell transplantation.

[PMID 17690160OA-icon.png] Raised interleukin-10 is an indicator of poor outcome and enhanced systemic inflammation in patients with acute coronary syndrome.

[PMID 18426996OA-icon.png] Relations of inflammatory biomarkers and common genetic variants with arterial stiffness and wave reflection.

[PMID 18479293OA-icon.png] Evaluation of IL10, IL19 and IL20 gene polymorphisms and chronic hepatitis B infection outcome.

[PMID 18520591OA-icon.png] Sequence variants in host cell factor C1 are associated with Meniere's disease.

[PMID 18640487OA-icon.png] Association of donor inflammation- and apoptosis-related genotypes and delayed allograft function after kidney transplantation.

[PMID 19468064OA-icon.png] Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions.

[PMID 19503741OA-icon.png] Coding variant Met72Thr in the PEDF gene and risk of neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.

[PMID 19505919OA-icon.png] Toll-like receptor signaling pathway variants and prostate cancer mortality.

[PMID 19753309OA-icon.png] SOD2 gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.

[PMID 19907653OA-icon.png] Selection for genetic variation inducing pro-inflammatory responses under adverse environmental conditions in a Ghanaian population.

[PMID 20416077OA-icon.png] Identification of type 2 diabetes-associated combination of SNPs using support vector machine.

[PMID 20525402OA-icon.png] Analysis of eight genes modulating interferon gamma and human genetic susceptibility to tuberculosis: a case-control association study.

[PMID 20617178OA-icon.png] Leprosy and the adaptation of human toll-like receptor 1.

[PMID 20622879] Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behcet's disease susceptibility loci.

[PMID 21532858OA-icon.png] Association of IL10, IL10RA, and IL10RB polymorphisms with benign prostate hyperplasia in Korean population.

[PMID 22378604] Association study of IL10 and IL23R-IL12RB2 in Iranian patients with Behcet's disease.


[PMID 24040186OA-icon.png] Relationship of serum interleukin-10 and its genetic variations with ischemic stroke in a chinese general population


[PMID 23096091] Association between IL10, IL10RA, and IL10RB SNPs and ischemic stroke with hypertension in Korean population.


[PMID 24903972] Genetic predisposition to calcific aortic stenosis and mitral annular calcification


[PMID 26015771OA-icon.png] Interleukin-10 gene polymorphisms are associated with Behcet's disease but not with Vogt-Koyanagi-Harada syndrome in the Chinese Han population