Rs11548605
From SNPedia
| Orientation | minus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11548605 |
| PheGenI | rs11548605 |
| nextbio | rs11548605 |
| hapmap | rs11548605 |
| 1000 genomes | rs11548605 |
| hgdp | rs11548605 |
| ensembl | rs11548605 |
| gopubmed | rs11548605 |
| geneview | rs11548605 |
| scholar | rs11548605 |
| rs11548605 | |
| pharmgkb | rs11548605 |
| gwascentral | rs11548605 |
| openSNP | rs11548605 |
| 23andMe | rs11548605 |
| 23andMe all | rs11548605 |
| SNP Nexus | |
| SNPshot | rs11548605 |
| SNPdbe | rs11548605 |
| MSV3d | rs11548605 |
| Gene | HBA1 |
| Chromosome | 16 |
| Orientation | minus |
| Position | 226780 |
| Reference | GRCh37.p5 37.3/135 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (G;G) | 0 | common in complete genomics |
| Make rs11548605(A;A) |
| Make rs11548605(A;C) |
| ClinVar | |
|---|---|
| Risk | rs11548605(A,G,T;A,G,T) |
| Normal | rs11548605(C;C) |
| Significance | 1 |
| Disease | |
| ClinVar | info |
| Gene | HBA1 |
| CLNDBN | |
| Reversed | 0 |
| CLNHGVS | NC_000016.9:g.226780C>A |
| CLNSRC | |