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rs3027898

From SNPedia

Orientationplus
Stabilizedplus
Make rs3027898(A;A)
Make rs3027898(A;C)
Make rs3027898(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154010439
GeneIRAK1
is asnp
is mentioned by
dbSNPrs3027898
dbSNP (classic)rs3027898
ClinGenrs3027898
ebirs3027898
HLIrs3027898
Exacrs3027898
Gnomadrs3027898
Varsomers3027898
LitVarrs3027898
Maprs3027898
PheGenIrs3027898
Biobankrs3027898
1000 genomesrs3027898
hgdprs3027898
ensemblrs3027898
geneviewrs3027898
scholarrs3027898
googlers3027898
pharmgkbrs3027898
gwascentralrs3027898
openSNPrs3027898
23andMers3027898
SNPshotrs3027898
SNPdbers3027898
MSV3drs3027898
GWAS Ctlgrs3027898
GMAF0.4407
Max Magnitude0
? (A;A) (A;C) (C;C) 28


The A->C rs3027898 polymorphism of the IRAK1 gene was significantly associated with atherothrombotic cerebral infarction in a study of 3,400+ Japanese adults.[PMID 18566305]


[PMID 20500689] The Role of microRNA-146a (miR-146a) and its Target IL-1R-Associated Kinase (IRAK1) in Psoriatic Arthritis Susceptibility

[PMID 20870441] A polymorphism in the 3'-UTR of interleukin-1 receptor-associated kinase (IRAK1), a target gene of miR-146a, is associated with rheumatoid arthritis susceptibility


[PMID 22451023] IRAK1 rs3027898 C/A polymorphism is associated with risk of rheumatoid arthritis

[PMID 17382928OA-icon.png] The association between innate immunity gene (IRAK1) and C-reactive protein in the Diabetes Heart Study.

[PMID 19717458OA-icon.png] A common MECP2 haplotype associates with reduced cortical surface area in humans in two independent populations.


[PMID 23435933] Association of interleukin-1 receptor-associated kinase (IRAK1) gene polymorphisms (rs3027898, rs1059702) with systemic lupus erythematosus in a Chinese Han population.


[PMID 25458699] Variants in IRAK1-MECP2 region confer susceptibility to autoimmune thyroid diseases


[PMID 26043172] Polymorphism of X-linked CD40 ligand gene associated with pulmonary tuberculosis in the Han Chinese population


[PMID 32173002] IRAK1 polymorphisms are associated with susceptibility to neuromyelitis optica spectrum disorder.