rs281864828
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs281864828(A;A) |
| Make rs281864828(A;T) |
| Make rs281864828(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 16 |
| Position | 173151 |
| Gene | HBA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs281864828 |
| dbSNP (classic) | rs281864828 |
| ClinGen | rs281864828 |
| ebi | rs281864828 |
| HLI | rs281864828 |
| Exac | rs281864828 |
| Gnomad | rs281864828 |
| Varsome | rs281864828 |
| LitVar | rs281864828 |
| Map | rs281864828 |
| PheGenI | rs281864828 |
| Biobank | rs281864828 |
| 1000 genomes | rs281864828 |
| hgdp | rs281864828 |
| ensembl | rs281864828 |
| geneview | rs281864828 |
| scholar | rs281864828 |
| rs281864828 | |
| pharmgkb | rs281864828 |
| gwascentral | rs281864828 |
| openSNP | rs281864828 |
| 23andMe | rs281864828 |
| SNPshot | rs281864828 |
| SNPdbe | rs281864828 |
| MSV3d | rs281864828 |
| GWAS Ctlg | rs281864828 |
| Max Magnitude | 0 |
OMIM pathogenic variant
