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rs4713693

From SNPedia

Orientationplus
Stabilizedplus
Make rs4713693(C;C)
Make rs4713693(C;T)
Make rs4713693(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position33850152
is asnp
is mentioned by
dbSNPrs4713693
ebirs4713693
HLIrs4713693
Exacrs4713693
Varsomers4713693
Maprs4713693
PheGenIrs4713693
hapmaprs4713693
1000 genomesrs4713693
hgdprs4713693
ensemblrs4713693
gopubmedrs4713693
geneviewrs4713693
scholarrs4713693
googlers4713693
pharmgkbrs4713693
gwascentralrs4713693
openSNPrs4713693
23andMers4713693
23andMe allrs4713693
SNP Nexus

SNPshotrs4713693
SNPdbers4713693
MSV3drs4713693
GWAS Ctlgrs4713693
GMAF0.4151
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21900946]
Trait
Title Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
Risk Allele T
P-val 7E-13
Odds Ratio 1.4000 [1.28-1.53]