rs1456893
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1456893(A;A) |
Make rs1456893(A;G) |
Make rs1456893(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 50230076 |
is a | snp |
is | mentioned by |
dbSNP | rs1456893 |
dbSNP (classic) | rs1456893 |
ClinGen | rs1456893 |
ebi | rs1456893 |
HLI | rs1456893 |
Exac | rs1456893 |
Gnomad | rs1456893 |
Varsome | rs1456893 |
LitVar | rs1456893 |
Map | rs1456893 |
PheGenI | rs1456893 |
Biobank | rs1456893 |
1000 genomes | rs1456893 |
hgdp | rs1456893 |
ensembl | rs1456893 |
geneview | rs1456893 |
scholar | rs1456893 |
rs1456893 | |
pharmgkb | rs1456893 |
gwascentral | rs1456893 |
openSNP | rs1456893 |
23andMe | rs1456893 |
SNPshot | rs1456893 |
SNPdbe | rs1456893 |
MSV3d | rs1456893 |
GWAS Ctlg | rs1456893 |
GMAF | 0.3857 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 18587394] |
Trait | Crohn's disease |
Title | Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease |
Risk Allele | A |
P-val | 5.0000000000000001E-9 |
Odds Ratio | 1.20 [NR] |
DeCode reports that rs1456893 is associated with susceptibility to Crohn's disease. [PMID 18587394]
[PMID 19068216] Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.
[PMID 21304977] An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.
[PMID 21830272] Distinct and overlapping genetic loci in Crohn's disease and ulcerative colitis: correlations with pathogenesis.