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rs1033180

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1033180(C;T)
Make rs1033180(T;T)
ReferenceGRCh37 37.1/131
Chromosome6
Position383546
is asnp
is mentioned by
dbSNPrs1033180
ebirs1033180
HLIrs1033180
Exacrs1033180
Varsomers1033180
Maprs1033180
PheGenIrs1033180
hapmaprs1033180
1000 genomesrs1033180
hgdprs1033180
ensemblrs1033180
gopubmedrs1033180
geneviewrs1033180
scholarrs1033180
googlers1033180
pharmgkbrs1033180
gwascentralrs1033180
openSNPrs1033180
23andMers1033180
23andMe allrs1033180
SNP Nexus

SNPshotrs1033180
SNPdbers1033180
MSV3drs1033180
GWAS Ctlgrs1033180
GMAF0.03214
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20190752OA-icon.png]
Trait Celiac disease
Title Multiple common variants for celiac disease influencing immune gene expression
Risk Allele A
P-val 6E-8
Odds Ratio 1.21 [1.13-1.29]