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rs6832151

From SNPedia

Orientationplus
Stabilizedplus
Make rs6832151(G;G)
Make rs6832151(G;T)
Make rs6832151(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position40301616
GeneLOC101930098
is asnp
is mentioned by
dbSNPrs6832151
ebirs6832151
HLIrs6832151
Exacrs6832151
Varsomers6832151
Maprs6832151
PheGenIrs6832151
hapmaprs6832151
1000 genomesrs6832151
hgdprs6832151
ensemblrs6832151
gopubmedrs6832151
geneviewrs6832151
scholarrs6832151
googlers6832151
pharmgkbrs6832151
gwascentralrs6832151
openSNPrs6832151
23andMers6832151
23andMe allrs6832151
SNP Nexus

SNPshotrs6832151
SNPdbers6832151
MSV3drs6832151
GWAS Ctlgrs6832151
GMAF0.2961
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 21841780]
Trait
Title A genome-wide association study identifies two new risk loci for Graves' disease.
Risk Allele G
P-val 1E-13
Odds Ratio 1.2400 [1.17-1.31]

[PMID 22489947] The replication of the association of the rs6832151 within chromosomal band 4p14 with Graves' disease in a Polish Caucasian population.