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rs4248154

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs4248154(C;T)
Make rs4248154(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31034839
GeneMUC22
is asnp
is mentioned by
dbSNPrs4248154
ebirs4248154
HLIrs4248154
Exacrs4248154
Varsomers4248154
Maprs4248154
PheGenIrs4248154
hapmaprs4248154
1000 genomesrs4248154
hgdprs4248154
ensemblrs4248154
gopubmedrs4248154
geneviewrs4248154
scholarrs4248154
googlers4248154
pharmgkbrs4248154
gwascentralrs4248154
openSNPrs4248154
23andMers4248154
23andMe allrs4248154
SNP Nexus

SNPshotrs4248154
SNPdbers4248154
MSV3drs4248154
GWAS Ctlgrs4248154
GMAF0.2043
Max Magnitude0
? (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 C
P-val 1E-13
Odds Ratio 1.3800 [1.27-1.50]