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rs4495224

From SNPedia

Orientationplus
Stabilizedplus
Make rs4495224(A;A)
Make rs4495224(A;C)
Make rs4495224(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position40477413
is asnp
is mentioned by
dbSNPrs4495224
ebirs4495224
HLIrs4495224
Exacrs4495224
Varsomers4495224
Maprs4495224
PheGenIrs4495224
hapmaprs4495224
1000 genomesrs4495224
hgdprs4495224
ensemblrs4495224
gopubmedrs4495224
geneviewrs4495224
scholarrs4495224
googlers4495224
pharmgkbrs4495224
gwascentralrs4495224
openSNPrs4495224
23andMers4495224
23andMe allrs4495224
SNP Nexus

SNPshotrs4495224
SNPdbers4495224
MSV3drs4495224
GWAS Ctlgrs4495224
GMAF0.4844
Max Magnitude
? (A;A) (A;C) (C;C) 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


[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.