Have questions? Visit https://www.reddit.com/r/SNPedia

rs1143630

From SNPedia

Orientationminus
Stabilizedminus
Make rs1143630(A;A)
Make rs1143630(A;C)
Make rs1143630(C;C)
ReferenceGRCh38 38.1/142
Chromosome2
Position112834078
GeneIL1B
is asnp
is mentioned by
dbSNPrs1143630
dbSNP (classic)rs1143630
ClinGenrs1143630
ebirs1143630
HLIrs1143630
Exacrs1143630
Gnomadrs1143630
Varsomers1143630
LitVarrs1143630
Maprs1143630
PheGenIrs1143630
Biobankrs1143630
1000 genomesrs1143630
hgdprs1143630
ensemblrs1143630
geneviewrs1143630
scholarrs1143630
googlers1143630
pharmgkbrs1143630
gwascentralrs1143630
openSNPrs1143630
23andMers1143630
SNPshotrs1143630
SNPdbers1143630
MSV3drs1143630
GWAS Ctlgrs1143630
GMAF0.1529
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 21726461OA-icon.png] Modulation of cortisol responses to the DEX/CRH test by polymorphisms of the interleukin-1beta gene in healthy adults


[PMID 21843369OA-icon.png] Possible association between Interleukin-1beta gene and schizophrenia in a Japanese population


[PMID 16508980] Association of the IL1 gene cluster with susceptibility to ankylosing spondylitis: an analysis of three Canadian populations.


[PMID 18573495OA-icon.png] IL1B genetic variation and plasma C-reactive protein level among young adults: the CARDIA study.


[PMID 19729864OA-icon.png] Association of genetic variation in serum amyloid-A with cardiovascular disease and interactions with IL6, IL1RN, IL1beta and TNF genes in the Cardiovascular Health Study.


[PMID 32391643] Evaluation of genetic variants in IL-1B and its interaction with the predisposition of osteoporosis in the northwestern Chinese Han population.