rs140029568
From SNPedia
| Merged into | rs41541519 |
| Orientation | minus |
| Stabilized | plus |
| Make rs140029568(A;A) |
| Make rs140029568(A;T) |
| Make rs140029568(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31356287 |
| Gene | HLA-B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs140029568 |
| dbSNP (classic) | rs140029568 |
| ClinGen | rs140029568 |
| ebi | rs140029568 |
| HLI | rs140029568 |
| Exac | rs140029568 |
| Gnomad | rs140029568 |
| Varsome | rs140029568 |
| LitVar | rs140029568 |
| Map | rs140029568 |
| PheGenI | rs140029568 |
| Biobank | rs140029568 |
| 1000 genomes | rs140029568 |
| hgdp | rs140029568 |
| ensembl | rs140029568 |
| geneview | rs140029568 |
| scholar | rs140029568 |
| rs140029568 | |
| pharmgkb | rs140029568 |
| gwascentral | rs140029568 |
| openSNP | rs140029568 |
| 23andMe | rs140029568 |
| SNPshot | rs140029568 |
| SNPdbe | rs140029568 |
| MSV3d | rs140029568 |
| GWAS Ctlg | rs140029568 |
| Status | Merged into rs41541519 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs140029568(A;A) |
| Alt | rs140029568(A;A) |
| Reference | rs140029568(T;T) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-B |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000006.11:g.31324064T>A |
| CLNSRC | |
| CLNACC | |
