rs112094427
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs112094427(A;A) |
| Make rs112094427(A;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 29943620 |
| Gene | HLA-A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs112094427 |
| dbSNP (classic) | rs112094427 |
| ClinGen | rs112094427 |
| ebi | rs112094427 |
| HLI | rs112094427 |
| Exac | rs112094427 |
| Gnomad | rs112094427 |
| Varsome | rs112094427 |
| LitVar | rs112094427 |
| Map | rs112094427 |
| PheGenI | rs112094427 |
| Biobank | rs112094427 |
| 1000 genomes | rs112094427 |
| hgdp | rs112094427 |
| ensembl | rs112094427 |
| geneview | rs112094427 |
| scholar | rs112094427 |
| rs112094427 | |
| pharmgkb | rs112094427 |
| gwascentral | rs112094427 |
| openSNP | rs112094427 |
| 23andMe | rs112094427 |
| SNPshot | rs112094427 |
| SNPdbe | rs112094427 |
| MSV3d | rs112094427 |
| GWAS Ctlg | rs112094427 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs112094427(A;A) |
| Alt | rs112094427(A;A) |
| Reference | Rs112094427(T;T) |
| Significance | Histocompatibility |
| Disease | |
| Variation | info |
| Gene | HLA-A |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000006.11:g.29911397T>A |
| CLNSRC | |
| CLNACC | |
