rs2019960
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2019960(C;C) |
| Make rs2019960(C;T) |
| Make rs2019960(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 128180025 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2019960 |
| dbSNP (classic) | rs2019960 |
| ClinGen | rs2019960 |
| ebi | rs2019960 |
| HLI | rs2019960 |
| Exac | rs2019960 |
| Gnomad | rs2019960 |
| Varsome | rs2019960 |
| LitVar | rs2019960 |
| Map | rs2019960 |
| PheGenI | rs2019960 |
| Biobank | rs2019960 |
| 1000 genomes | rs2019960 |
| hgdp | rs2019960 |
| ensembl | rs2019960 |
| geneview | rs2019960 |
| scholar | rs2019960 |
| rs2019960 | |
| pharmgkb | rs2019960 |
| gwascentral | rs2019960 |
| openSNP | rs2019960 |
| 23andMe | rs2019960 |
| SNPshot | rs2019960 |
| SNPdbe | rs2019960 |
| MSV3d | rs2019960 |
| GWAS Ctlg | rs2019960 |
| GMAF | 0.2433 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21037568
] A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3)
| GWAS snp | |
|---|---|
| PMID | [PMID 21833088 |
| Trait | |
| Title | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
| Risk Allele | G |
| P-val | 5E-9 |
| Odds Ratio | 1.1200 [1.10-1.13] |
| 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 | 6E-10 |
| Odds Ratio | 1.37 [NR] |
| GWAS snp | |
|---|---|
| PMID | [PMID 24920014 |
| Trait | Hodgkin's lymphoma |
| Title | A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus. |
| Risk Allele | C |
| P-val | 7E-8 |
| Odds Ratio | 1.30 [1.181.43] |
