rs8176694
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs8176694(A;A) |
| Make rs8176694(A;G) |
| Make rs8176694(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 133262243 |
| Gene | ABO |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8176694 |
| dbSNP (classic) | rs8176694 |
| ClinGen | rs8176694 |
| ebi | rs8176694 |
| HLI | rs8176694 |
| Exac | rs8176694 |
| Gnomad | rs8176694 |
| Varsome | rs8176694 |
| LitVar | rs8176694 |
| Map | rs8176694 |
| PheGenI | rs8176694 |
| Biobank | rs8176694 |
| 1000 genomes | rs8176694 |
| hgdp | rs8176694 |
| ensembl | rs8176694 |
| geneview | rs8176694 |
| scholar | rs8176694 |
| rs8176694 | |
| pharmgkb | rs8176694 |
| gwascentral | rs8176694 |
| openSNP | rs8176694 |
| 23andMe | rs8176694 |
| SNPshot | rs8176694 |
| SNPdbe | rs8176694 |
| MSV3d | rs8176694 |
| GWAS Ctlg | rs8176694 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
This SNP is a variant in the ABO gene, and is therefore potentially useful in determining ABO blood group, such as through the use of genosets.
[PMID 32293292
] Susceptible gene polymorphism in patients with three-vessel coronary artery disease.
