rs783396
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs783396(A;A) |
| Make rs783396(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 106539495 |
| Gene | AIM1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs783396 |
| dbSNP (classic) | rs783396 |
| ClinGen | rs783396 |
| ebi | rs783396 |
| HLI | rs783396 |
| Exac | rs783396 |
| Gnomad | rs783396 |
| Varsome | rs783396 |
| LitVar | rs783396 |
| Map | rs783396 |
| PheGenI | rs783396 |
| Biobank | rs783396 |
| 1000 genomes | rs783396 |
| hgdp | rs783396 |
| ensembl | rs783396 |
| geneview | rs783396 |
| scholar | rs783396 |
| rs783396 | |
| pharmgkb | rs783396 |
| gwascentral | rs783396 |
| openSNP | rs783396 |
| 23andMe | rs783396 |
| SNPshot | rs783396 |
| SNPdbe | rs783396 |
| MSV3d | rs783396 |
| GWAS Ctlg | rs783396 |
| GMAF | 0.07208 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs783396 |
| PubMedID | [PMID 17434096 ]
|
| Condition | Stroke |
| Gene | AIM1 |
| Risk Allele | |
| pValue | 9.00E-006 |
| OR | 2.17 |
| 95% CI | 1.47-3.13 |
[PMID 22403240] Associations Between Incident Ischemic Stroke Events and Stroke and Cardiovascular Disease-Related GWAS SNPs in the Population Architecture Using Genomics and Epidemiology (PAGE) Study
