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rs3213448

From SNPedia

Orientationplus
Stabilizedplus
Make rs3213448(A;A)
Make rs3213448(A;G)
Make rs3213448(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position113121720
GeneIL1RN
is asnp
is mentioned by
dbSNPrs3213448
ebirs3213448
HLIrs3213448
Exacrs3213448
Varsomers3213448
Maprs3213448
PheGenIrs3213448
hapmaprs3213448
1000 genomesrs3213448
hgdprs3213448
ensemblrs3213448
gopubmedrs3213448
geneviewrs3213448
scholarrs3213448
googlers3213448
pharmgkbrs3213448
gwascentralrs3213448
openSNPrs3213448
23andMers3213448
23andMe allrs3213448
SNP Nexus

SNPshotrs3213448
SNPdbers3213448
MSV3drs3213448
GWAS Ctlgrs3213448
GMAF0.2893
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 20178882] Genetic variation of the interleukin-1 family and nongenetic factors determining the interleukin-1 receptor antagonist phenotypes


[PMID 18451331OA-icon.png] Polymorphisms of the IL1-receptor antagonist gene (IL1RN) are associated with multiple markers of systemic inflammation.


[PMID 19567509OA-icon.png] Genetic variants and prostate cancer risk: candidate replication and exploration of viral restriction genes.


[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 21205020] Associations between interleukin-1 (IL-1) gene variations or IL-1 receptor antagonist levels and the development of type 2 diabetes.