rs1140487
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs1140487(A;A) |
| Make rs1140487(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31355210 |
| Gene | HLA-B, MIR6891 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1140487 |
| dbSNP (classic) | rs1140487 |
| ClinGen | rs1140487 |
| ebi | rs1140487 |
| HLI | rs1140487 |
| Exac | rs1140487 |
| Gnomad | rs1140487 |
| Varsome | rs1140487 |
| LitVar | rs1140487 |
| Map | rs1140487 |
| PheGenI | rs1140487 |
| Biobank | rs1140487 |
| 1000 genomes | rs1140487 |
| hgdp | rs1140487 |
| ensembl | rs1140487 |
| geneview | rs1140487 |
| scholar | rs1140487 |
| rs1140487 | |
| pharmgkb | rs1140487 |
| gwascentral | rs1140487 |
| openSNP | rs1140487 |
| 23andMe | rs1140487 |
| SNPshot | rs1140487 |
| SNPdbe | rs1140487 |
| MSV3d | rs1140487 |
| GWAS Ctlg | rs1140487 |
| GMAF | 0.03122 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs1140487(A;A) |
| Alt | rs1140487(A;A) |
| Reference | Rs1140487(G;G) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-B |
| CLNDBN | |
| Reversed | 1 |
| HGVS | NC_000006.11:g.31322987C>T |
| CLNSRC | |
| CLNACC | |
