rs1036935
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1036935(C;C) |
| Make rs1036935(C;T) |
| Make rs1036935(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 18 |
| Position | 50317164 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1036935 |
| dbSNP (classic) | rs1036935 |
| ClinGen | rs1036935 |
| ebi | rs1036935 |
| HLI | rs1036935 |
| Exac | rs1036935 |
| Gnomad | rs1036935 |
| Varsome | rs1036935 |
| LitVar | rs1036935 |
| Map | rs1036935 |
| PheGenI | rs1036935 |
| Biobank | rs1036935 |
| 1000 genomes | rs1036935 |
| hgdp | rs1036935 |
| ensembl | rs1036935 |
| geneview | rs1036935 |
| scholar | rs1036935 |
| rs1036935 | |
| pharmgkb | rs1036935 |
| gwascentral | rs1036935 |
| openSNP | rs1036935 |
| 23andMe | rs1036935 |
| SNPshot | rs1036935 |
| SNPdbe | rs1036935 |
| MSV3d | rs1036935 |
| GWAS Ctlg | rs1036935 |
| GMAF | 0.1896 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20062064 ]
|
| Trait | Chronic lymphocytic leukemia |
| Title | Common variants at 2q37.3, 8q24.21, 15q21.3 abd 16q24.1 influence chronic lymphocytic leukemia risk |
| Risk Allele | T |
| P-val | 0.000002 |
| Odds Ratio | 1.22 [1.12-1.32] |
[PMID 21554262] Common genetic variation at 15q25.2 impacts on chronic lymphocytic leukaemia risk.
