rs1253871
From SNPedia
| Merged into | rs819760 |
| Orientation | plus |
| Stabilized | plus |
| Make rs1253871(C;C) |
| Make rs1253871(C;T) |
| Make rs1253871(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 1 |
| Position | 99244586 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1253871 |
| dbSNP (classic) | rs1253871 |
| ClinGen | rs1253871 |
| ebi | rs1253871 |
| HLI | rs1253871 |
| Exac | rs1253871 |
| Gnomad | rs1253871 |
| Varsome | rs1253871 |
| LitVar | rs1253871 |
| Map | rs1253871 |
| PheGenI | rs1253871 |
| Biobank | rs1253871 |
| 1000 genomes | rs1253871 |
| hgdp | rs1253871 |
| ensembl | rs1253871 |
| geneview | rs1253871 |
| scholar | rs1253871 |
| rs1253871 | |
| pharmgkb | rs1253871 |
| gwascentral | rs1253871 |
| openSNP | rs1253871 |
| 23andMe | rs1253871 |
| SNPshot | rs1253871 |
| SNPdbe | rs1253871 |
| MSV3d | rs1253871 |
| GWAS Ctlg | rs1253871 |
| Status | Merged into rs819760 |
| Max Magnitude | 0 |
[PMID 25511740
] Identification of epidermal growth factor receptor (EGFR) genetic variants that modify risk for head and neck squamous cell carcinoma
