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rs2069779

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2069779(C;T)
Make rs2069779(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position122452742
GeneIL2
is asnp
is mentioned by
dbSNPrs2069779
ebirs2069779
HLIrs2069779
Exacrs2069779
Varsomers2069779
Maprs2069779
PheGenIrs2069779
hapmaprs2069779
1000 genomesrs2069779
hgdprs2069779
ensemblrs2069779
gopubmedrs2069779
geneviewrs2069779
scholarrs2069779
googlers2069779
pharmgkbrs2069779
gwascentralrs2069779
openSNPrs2069779
23andMers2069779
23andMe allrs2069779
SNP Nexus

SNPshotrs2069779
SNPdbers2069779
MSV3drs2069779
GWAS Ctlgrs2069779
GMAF0.03673
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 21736829] Gene-PUFA interactions and obesity risk