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rs1427676

From SNPedia

Orientationplus
Stabilizedplus
Make rs1427676(C;C)
Make rs1427676(C;T)
Make rs1427676(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position203876443
is asnp
is mentioned by
dbSNPrs1427676
ebirs1427676
HLIrs1427676
Exacrs1427676
Varsomers1427676
Maprs1427676
PheGenIrs1427676
hapmaprs1427676
1000 genomesrs1427676
hgdprs1427676
ensemblrs1427676
gopubmedrs1427676
geneviewrs1427676
scholarrs1427676
googlers1427676
pharmgkbrs1427676
gwascentralrs1427676
openSNPrs1427676
23andMers1427676
23andMe allrs1427676
SNP Nexus

SNPshotrs1427676
SNPdbers1427676
MSV3drs1427676
GWAS Ctlgrs1427676
GMAF0.4582
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19956106OA-icon.png] Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families


[PMID 19956097OA-icon.png] Remapping the type I diabetes association of the CTLA4 locus.


[PMID 19956101OA-icon.png] Overview of the Rapid Response data.


[PMID 20537165OA-icon.png] The CTLA4 variants may interact with the IL23R- and NOD2-conferred risk in development of Crohn's disease.