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rs5912838

From SNPedia

Orientationplus
Stabilizedplus
Make rs5912838(A;A)
Make rs5912838(A;C)
Make rs5912838(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position79241621
is asnp
is mentioned by
dbSNPrs5912838
ebirs5912838
HLIrs5912838
Exacrs5912838
Varsomers5912838
Maprs5912838
PheGenIrs5912838
hapmaprs5912838
1000 genomesrs5912838
hgdprs5912838
ensemblrs5912838
gopubmedrs5912838
geneviewrs5912838
scholarrs5912838
googlers5912838
pharmgkbrs5912838
gwascentralrs5912838
openSNPrs5912838
23andMers5912838
23andMe allrs5912838
SNP Nexus

SNPshotrs5912838
SNPdbers5912838
MSV3drs5912838
GWAS Ctlgrs5912838
GMAF0.4849
Max Magnitude
? (A;A) (A;C) (C;C) 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 2E-33
Odds Ratio 1.32 [1.25-1.37]


[PMID 23667180OA-icon.png] An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease.