rs1869839
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1869839(A;A) |
Make rs1869839(A;G) |
Make rs1869839(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 114717488 |
is a | snp |
is | mentioned by |
dbSNP | rs1869839 |
dbSNP (classic) | rs1869839 |
ClinGen | rs1869839 |
ebi | rs1869839 |
HLI | rs1869839 |
Exac | rs1869839 |
Gnomad | rs1869839 |
Varsome | rs1869839 |
LitVar | rs1869839 |
Map | rs1869839 |
PheGenI | rs1869839 |
Biobank | rs1869839 |
1000 genomes | rs1869839 |
hgdp | rs1869839 |
ensembl | rs1869839 |
geneview | rs1869839 |
scholar | rs1869839 |
rs1869839 | |
pharmgkb | rs1869839 |
gwascentral | rs1869839 |
openSNP | rs1869839 |
23andMe | rs1869839 |
SNPshot | rs1869839 |
SNPdbe | rs1869839 |
MSV3d | rs1869839 |
GWAS Ctlg | rs1869839 |
GMAF | 0.2089 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22936669] |
Trait | Crohn's disease |
Title | A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. |
Risk Allele | |
P-val | 7E-6 |
Odds Ratio | 1.20 [1.11-1.3] |