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rs296547

From SNPedia

Orientationminus
Stabilizedminus
Make rs296547(A;A)
Make rs296547(A;G)
Make rs296547(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position200923009
is asnp
is mentioned by
dbSNPrs296547
ebirs296547
HLIrs296547
Exacrs296547
Varsomers296547
Maprs296547
PheGenIrs296547
hapmaprs296547
1000 genomesrs296547
hgdprs296547
ensemblrs296547
gopubmedrs296547
geneviewrs296547
scholarrs296547
googlers296547
pharmgkbrs296547
gwascentralrs296547
openSNPrs296547
23andMers296547
23andMe allrs296547
SNP Nexus

SNPshotrs296547
SNPdbers296547
MSV3drs296547
GWAS Ctlgrs296547
GMAF0.4945
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20190752OA-icon.png]
Trait Celiac disease
Title Multiple common variants for celiac disease influencing immune gene expression
Risk Allele
P-val 4E-9
Odds Ratio 1.12 [1.09-1.16]

[PMID 21437271OA-icon.png] Genome-wide interaction-based association analysis identified multiple new susceptibility Loci for common diseases.


[PMID 24871462] Coeliac disease-associated polymorphisms influence thymic gene expression