rs11229030
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 2 | higher odds of Crohn's disease |
Make rs11229030(C;T) |
Make rs11229030(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 57435536 |
is a | snp |
is | mentioned by |
dbSNP | rs11229030 |
dbSNP (classic) | rs11229030 |
ClinGen | rs11229030 |
ebi | rs11229030 |
HLI | rs11229030 |
Exac | rs11229030 |
Gnomad | rs11229030 |
Varsome | rs11229030 |
LitVar | rs11229030 |
Map | rs11229030 |
PheGenI | rs11229030 |
Biobank | rs11229030 |
1000 genomes | rs11229030 |
hgdp | rs11229030 |
ensembl | rs11229030 |
geneview | rs11229030 |
scholar | rs11229030 |
rs11229030 | |
pharmgkb | rs11229030 |
gwascentral | rs11229030 |
openSNP | rs11229030 |
23andMe | rs11229030 |
SNPshot | rs11229030 |
SNPdbe | rs11229030 |
MSV3d | rs11229030 |
GWAS Ctlg | rs11229030 |
GMAF | 0.36 |
Max Magnitude | 2 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22412388] A genome-wide scan of ashkenazi jewish Crohn's disease suggests novel susceptibility Loci.