rs4495224
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4495224(A;A) |
Make rs4495224(A;C) |
Make rs4495224(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 40477413 |
is a | snp |
is | mentioned by |
dbSNP | rs4495224 |
dbSNP (classic) | rs4495224 |
ClinGen | rs4495224 |
ebi | rs4495224 |
HLI | rs4495224 |
Exac | rs4495224 |
Gnomad | rs4495224 |
Varsome | rs4495224 |
LitVar | rs4495224 |
Map | rs4495224 |
PheGenI | rs4495224 |
Biobank | rs4495224 |
1000 genomes | rs4495224 |
hgdp | rs4495224 |
ensembl | rs4495224 |
geneview | rs4495224 |
scholar | rs4495224 |
rs4495224 | |
pharmgkb | rs4495224 |
gwascentral | rs4495224 |
openSNP | rs4495224 |
23andMe | rs4495224 |
SNPshot | rs4495224 |
SNPdbe | rs4495224 |
MSV3d | rs4495224 |
GWAS Ctlg | rs4495224 |
GMAF | 0.4844 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 23300802] PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites
[PMID 17447842] Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.