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rs2294025

From SNPedia

Orientationplus
Stabilizedplus
Make rs2294025(A;A)
Make rs2294025(A;G)
Make rs2294025(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position133133268
GeneTG
is asnp
is mentioned by
dbSNPrs2294025
ebirs2294025
HLIrs2294025
Exacrs2294025
Varsomers2294025
Maprs2294025
PheGenIrs2294025
hapmaprs2294025
1000 genomesrs2294025
hgdprs2294025
ensemblrs2294025
gopubmedrs2294025
geneviewrs2294025
scholarrs2294025
googlers2294025
pharmgkbrs2294025
gwascentralrs2294025
openSNPrs2294025
23andMers2294025
23andMe allrs2294025
SNP Nexus

SNPshotrs2294025
SNPdbers2294025
MSV3drs2294025
GWAS Ctlgrs2294025
GMAF0.4151
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23612905]
Trait Graves' disease
Title Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
Risk Allele T
P-val 8E-9
Odds Ratio 1.16 [1.10-1.22]