rs2371685
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2371685(A;A) |
| Make rs2371685(A;T) |
| Make rs2371685(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 40392124 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2371685 |
| dbSNP (classic) | rs2371685 |
| ClinGen | rs2371685 |
| ebi | rs2371685 |
| HLI | rs2371685 |
| Exac | rs2371685 |
| Gnomad | rs2371685 |
| Varsome | rs2371685 |
| LitVar | rs2371685 |
| Map | rs2371685 |
| PheGenI | rs2371685 |
| Biobank | rs2371685 |
| 1000 genomes | rs2371685 |
| hgdp | rs2371685 |
| ensembl | rs2371685 |
| geneview | rs2371685 |
| scholar | rs2371685 |
| rs2371685 | |
| pharmgkb | rs2371685 |
| gwascentral | rs2371685 |
| openSNP | rs2371685 |
| 23andMe | rs2371685 |
| SNPshot | rs2371685 |
| SNPdbe | rs2371685 |
| MSV3d | rs2371685 |
| GWAS Ctlg | rs2371685 |
| GMAF | 0.1097 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
| Rs2371685 | |
|---|---|
| PubMed | [PMID 17447842 ]
|
| Affy Probeset | SNP_A-4264860 |
| Affy Orientation | same |
| On GW 5.0 | 1 |
| Alleles A/B | A/T |
| Ancestral | A |
| Population | EU |
| Allele | T |
| Case Freq. | 0.19 |
| Control Freq. | 0.13 |
| Odds Ratio Het | |
| Odds Ratio Hom | |
| Odds Ratio All | 1.56 |
| Disease | Crohn's disease (CD) |
rs2371685 is in linkage disequilibrium with a polymorphism that increases susceptibility to Crohn's disease 1.56 times for carriers of the T allele [PMID 17447842]
[PMID 17903294] Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.
