rs574347
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs574347(C;C) |
| Make rs574347(C;T) |
| Make rs574347(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 133260255 |
| Gene | ABO |
| is a | snp |
| is | mentioned by |
| dbSNP | rs574347 |
| dbSNP (classic) | rs574347 |
| ClinGen | rs574347 |
| ebi | rs574347 |
| HLI | rs574347 |
| Exac | rs574347 |
| Gnomad | rs574347 |
| Varsome | rs574347 |
| LitVar | rs574347 |
| Map | rs574347 |
| PheGenI | rs574347 |
| Biobank | rs574347 |
| 1000 genomes | rs574347 |
| hgdp | rs574347 |
| ensembl | rs574347 |
| geneview | rs574347 |
| scholar | rs574347 |
| rs574347 | |
| pharmgkb | rs574347 |
| gwascentral | rs574347 |
| openSNP | rs574347 |
| 23andMe | rs574347 |
| SNPshot | rs574347 |
| SNPdbe | rs574347 |
| MSV3d | rs574347 |
| GWAS Ctlg | rs574347 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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.
