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rs743776

From SNPedia

Orientationplus
Stabilizedplus
Make rs743776(C;C)
Make rs743776(C;T)
Make rs743776(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position37155447
is asnp
is mentioned by
dbSNPrs743776
ebirs743776
HLIrs743776
Exacrs743776
Varsomers743776
Maprs743776
PheGenIrs743776
hapmaprs743776
1000 genomesrs743776
hgdprs743776
ensemblrs743776
gopubmedrs743776
geneviewrs743776
scholarrs743776
googlers743776
pharmgkbrs743776
gwascentralrs743776
openSNPrs743776
23andMers743776
23andMe allrs743776
SNP Nexus

SNPshotrs743776
SNPdbers743776
MSV3drs743776
GWAS Ctlgrs743776
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 23972291] Polymorphisms in the IL2RA and IL2RB genes in inflammatory bowel disease risk