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rs7720838

From SNPedia

Orientationplus
Stabilizedplus
Make rs7720838(G;G)
Make rs7720838(G;T)
Make rs7720838(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position40486794
is asnp
is mentioned by
dbSNPrs7720838
ebirs7720838
HLIrs7720838
Exacrs7720838
Varsomers7720838
Maprs7720838
PheGenIrs7720838
hapmaprs7720838
1000 genomesrs7720838
hgdprs7720838
ensemblrs7720838
gopubmedrs7720838
geneviewrs7720838
scholarrs7720838
googlers7720838
pharmgkbrs7720838
gwascentralrs7720838
openSNPrs7720838
23andMers7720838
23andMe allrs7720838
SNP Nexus

SNPshotrs7720838
SNPdbers7720838
MSV3drs7720838
GWAS Ctlgrs7720838
GMAF0.4206
Max Magnitude
? (G;G) (G;T) (T;T) 28
[PMID 23300802OA-icon.png] PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites
GWAS snp
PMID [PMID 23817569OA-icon.png]
Trait Self-reported allergy
Title A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.
Risk Allele G
P-val 8E-11
Odds Ratio .08 [0.055-0.102] unit decrease


[PMID 17447842OA-icon.png] Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.