rs11757919
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs11757919(A;A) |
| Make rs11757919(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31270069 |
| Gene | HLA-C |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11757919 |
| dbSNP (classic) | rs11757919 |
| ClinGen | rs11757919 |
| ebi | rs11757919 |
| HLI | rs11757919 |
| Exac | rs11757919 |
| Gnomad | rs11757919 |
| Varsome | rs11757919 |
| LitVar | rs11757919 |
| Map | rs11757919 |
| PheGenI | rs11757919 |
| Biobank | rs11757919 |
| 1000 genomes | rs11757919 |
| hgdp | rs11757919 |
| ensembl | rs11757919 |
| geneview | rs11757919 |
| scholar | rs11757919 |
| rs11757919 | |
| pharmgkb | rs11757919 |
| gwascentral | rs11757919 |
| openSNP | rs11757919 |
| 23andMe | rs11757919 |
| SNPshot | rs11757919 |
| SNPdbe | rs11757919 |
| MSV3d | rs11757919 |
| GWAS Ctlg | rs11757919 |
| GMAF | 0.009642 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs11757919(A;A) |
| Alt | rs11757919(A;A) |
| Reference | Rs11757919(G;G) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-C |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000006.11:g.31237846G>A |
| CLNSRC | |
| CLNACC | |
