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rs1456988

From SNPedia

Orientationplus
Stabilizedplus
Make rs1456988(G;G)
Make rs1456988(G;T)
Make rs1456988(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position98021670
is asnp
is mentioned by
dbSNPrs1456988
ebirs1456988
HLIrs1456988
Exacrs1456988
Varsomers1456988
Maprs1456988
PheGenIrs1456988
hapmaprs1456988
1000 genomesrs1456988
hgdprs1456988
ensemblrs1456988
gopubmedrs1456988
geneviewrs1456988
scholarrs1456988
googlers1456988
pharmgkbrs1456988
gwascentralrs1456988
openSNPrs1456988
23andMers1456988
23andMe allrs1456988
SNP Nexus

SNPshotrs1456988
SNPdbers1456988
MSV3drs1456988
GWAS Ctlgrs1456988
GMAF0.4192
Max Magnitude
? (G;G) (G;T) (T;T) 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
P-val 5E-9
Odds Ratio 1.12 [1.09-1.18]