rs9510787
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9510787(A;A) |
| Make rs9510787(A;G) |
| Make rs9510787(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 23631056 |
| Gene | TNFRSF19 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9510787 |
| dbSNP (classic) | rs9510787 |
| ClinGen | rs9510787 |
| ebi | rs9510787 |
| HLI | rs9510787 |
| Exac | rs9510787 |
| Gnomad | rs9510787 |
| Varsome | rs9510787 |
| LitVar | rs9510787 |
| Map | rs9510787 |
| PheGenI | rs9510787 |
| Biobank | rs9510787 |
| 1000 genomes | rs9510787 |
| hgdp | rs9510787 |
| ensembl | rs9510787 |
| geneview | rs9510787 |
| scholar | rs9510787 |
| rs9510787 | |
| pharmgkb | rs9510787 |
| gwascentral | rs9510787 |
| openSNP | rs9510787 |
| 23andMe | rs9510787 |
| SNPshot | rs9510787 |
| SNPdbe | rs9510787 |
| MSV3d | rs9510787 |
| GWAS Ctlg | rs9510787 |
| GMAF | 0.1965 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20512145] |
| Trait | Nasopharyngeal carcinoma |
| Title | A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. |
| Risk Allele | G |
| P-val | 2E-9 |
| Odds Ratio | 1.20 [1.10-1.30] |
The G allele of this SNP in the TNFRSF19 gene is associated with higher odds of nasopharyngeal cancer in people of southern Chinese descent. [PMID 20512145]
[PMID 27517745] Nasopharyngeal carcinoma risk prediction via salivary detection of host and Epstein-Barr virus genetic variants.
[PMID 30126334] Systematic Review and Meta-analysis of SNPs from Genome-Wide Association Studies of Head and Neck Cancer.
