rs11571378
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs11571378(A;A) |
| Make rs11571378(A;T) |
| Make rs11571378(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 950115 |
| Gene | RAD52 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11571378 |
| dbSNP (classic) | rs11571378 |
| ClinGen | rs11571378 |
| ebi | rs11571378 |
| HLI | rs11571378 |
| Exac | rs11571378 |
| Gnomad | rs11571378 |
| Varsome | rs11571378 |
| LitVar | rs11571378 |
| Map | rs11571378 |
| PheGenI | rs11571378 |
| Biobank | rs11571378 |
| 1000 genomes | rs11571378 |
| hgdp | rs11571378 |
| ensembl | rs11571378 |
| geneview | rs11571378 |
| scholar | rs11571378 |
| rs11571378 | |
| pharmgkb | rs11571378 |
| gwascentral | rs11571378 |
| openSNP | rs11571378 |
| 23andMe | rs11571378 |
| SNPshot | rs11571378 |
| SNPdbe | rs11571378 |
| MSV3d | rs11571378 |
| GWAS Ctlg | rs11571378 |
| Max Magnitude | 0 |
[PMID 25012956] A RAD52 genetic variant located in a miRNA binding site is associated with glioma risk in Han Chinese
[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.
