rs1250550
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1250550(G;G) |
Make rs1250550(G;T) |
Make rs1250550(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 79300560 |
Gene | ZMIZ1 |
is a | snp |
is | mentioned by |
dbSNP | rs1250550 |
dbSNP (classic) | rs1250550 |
ClinGen | rs1250550 |
ebi | rs1250550 |
HLI | rs1250550 |
Exac | rs1250550 |
Gnomad | rs1250550 |
Varsome | rs1250550 |
LitVar | rs1250550 |
Map | rs1250550 |
PheGenI | rs1250550 |
Biobank | rs1250550 |
1000 genomes | rs1250550 |
hgdp | rs1250550 |
ensembl | rs1250550 |
geneview | rs1250550 |
scholar | rs1250550 |
rs1250550 | |
pharmgkb | rs1250550 |
gwascentral | rs1250550 |
openSNP | rs1250550 |
23andMe | rs1250550 |
SNPshot | rs1250550 |
SNPdbe | rs1250550 |
MSV3d | rs1250550 |
GWAS Ctlg | rs1250550 |
GMAF | 0.2952 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19915574![]() |
Trait | Inflammatory bowel disease (early onset) |
Title | Common variants at five new loci associated with early-onset inflammatory bowel disease |
Risk Allele | |
P-val | 6E-9 |
Odds Ratio | 1.16 [1.09-1.25] |
[PMID 20473688] Association between genome-wide association studies reported SNPs and pediatric-onset Crohn's disease in Canadian children
GWAS snp | |
---|---|
PMID | [PMID 21102463![]() |
Trait | |
Title | Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci |
Risk Allele | G |
P-val | 1E-30 |
Odds Ratio | 1.1900 [1.15-1.23] |
[PMID 17068223] A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
GWAS snp | |
---|---|
PMID | [PMID 21833088![]() |
Trait | Multiple sclerosis |
Title | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
Risk Allele | A |
P-val | 6E-9 |
Odds Ratio | 1.10 [1.09-1.12] |
[PMID 23543094] Testing for associations between loci and environmental gradients using latent factor mixed models.