rs10849605
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10849605(C;C) |
| Make rs10849605(C;T) |
| Make rs10849605(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 955272 |
| Gene | RAD52 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10849605 |
| dbSNP (classic) | rs10849605 |
| ClinGen | rs10849605 |
| ebi | rs10849605 |
| HLI | rs10849605 |
| Exac | rs10849605 |
| Gnomad | rs10849605 |
| Varsome | rs10849605 |
| LitVar | rs10849605 |
| Map | rs10849605 |
| PheGenI | rs10849605 |
| Biobank | rs10849605 |
| 1000 genomes | rs10849605 |
| hgdp | rs10849605 |
| ensembl | rs10849605 |
| geneview | rs10849605 |
| scholar | rs10849605 |
| rs10849605 | |
| pharmgkb | rs10849605 |
| gwascentral | rs10849605 |
| openSNP | rs10849605 |
| 23andMe | rs10849605 |
| SNPshot | rs10849605 |
| SNPdbe | rs10849605 |
| MSV3d | rs10849605 |
| GWAS Ctlg | rs10849605 |
| GMAF | 0.4486 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22899653 ]
|
| Trait | Lung cancer |
| Title | Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls. |
| Risk Allele | |
| P-val | 6E-7 |
| Odds Ratio | 1.08 [1.04-1.11] |
[PMID 20805886] Unique DNA repair gene variations and potential associations with the primary antibody deficiency syndromes IgAD and CVID.
[PMID 25793373] The 12p13.33/RAD52 Locus and Genetic Susceptibility to Squamous Cell Cancers of Upper Aerodigestive Tract
[PMID 26629180] Identification of an SCLC susceptibility rs7963551 genetic polymorphism in a previously GWAS-identified 12p13.33 RAD52 lung cancer risk locus in the Chinese population.
