rs41553131
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs41553131(G;G) |
| Make rs41553131(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 29945031 |
| Gene | HLA-A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs41553131 |
| dbSNP (classic) | rs41553131 |
| ClinGen | rs41553131 |
| ebi | rs41553131 |
| HLI | rs41553131 |
| Exac | rs41553131 |
| Gnomad | rs41553131 |
| Varsome | rs41553131 |
| LitVar | rs41553131 |
| Map | rs41553131 |
| PheGenI | rs41553131 |
| Biobank | rs41553131 |
| 1000 genomes | rs41553131 |
| hgdp | rs41553131 |
| ensembl | rs41553131 |
| geneview | rs41553131 |
| scholar | rs41553131 |
| rs41553131 | |
| pharmgkb | rs41553131 |
| gwascentral | rs41553131 |
| openSNP | rs41553131 |
| 23andMe | rs41553131 |
| SNPshot | rs41553131 |
| SNPdbe | rs41553131 |
| MSV3d | rs41553131 |
| GWAS Ctlg | rs41553131 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs41553131(G;G) |
| Alt | rs41553131(G;G) |
| Reference | Rs41553131(T;T) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-A |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000006.11:g.29912808T>G |
| CLNSRC | |
| CLNACC | |
