rs7745098
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7745098(C;C) |
| Make rs7745098(C;T) |
| Make rs7745098(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 135093866 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7745098 |
| dbSNP (classic) | rs7745098 |
| ClinGen | rs7745098 |
| ebi | rs7745098 |
| HLI | rs7745098 |
| Exac | rs7745098 |
| Gnomad | rs7745098 |
| Varsome | rs7745098 |
| LitVar | rs7745098 |
| Map | rs7745098 |
| PheGenI | rs7745098 |
| Biobank | rs7745098 |
| 1000 genomes | rs7745098 |
| hgdp | rs7745098 |
| ensembl | rs7745098 |
| geneview | rs7745098 |
| scholar | rs7745098 |
| rs7745098 | |
| pharmgkb | rs7745098 |
| gwascentral | rs7745098 |
| openSNP | rs7745098 |
| 23andMe | rs7745098 |
| SNPshot | rs7745098 |
| SNPdbe | rs7745098 |
| MSV3d | rs7745098 |
| GWAS Ctlg | rs7745098 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24149102 ]
|
| Trait | Hodgkin's lymphoma |
| Title | Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. |
| Risk Allele | G |
| P-val | 3E-9 |
| Odds Ratio | 1.21 [1.14-1.29] |
