rs7963551
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7963551(G;G) |
| Make rs7963551(G;T) |
| Make rs7963551(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 912349 |
| Gene | RAD52 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7963551 |
| dbSNP (classic) | rs7963551 |
| ClinGen | rs7963551 |
| ebi | rs7963551 |
| HLI | rs7963551 |
| Exac | rs7963551 |
| Gnomad | rs7963551 |
| Varsome | rs7963551 |
| LitVar | rs7963551 |
| Map | rs7963551 |
| PheGenI | rs7963551 |
| Biobank | rs7963551 |
| 1000 genomes | rs7963551 |
| hgdp | rs7963551 |
| ensembl | rs7963551 |
| geneview | rs7963551 |
| scholar | rs7963551 |
| rs7963551 | |
| pharmgkb | rs7963551 |
| gwascentral | rs7963551 |
| openSNP | rs7963551 |
| 23andMe | rs7963551 |
| SNPshot | rs7963551 |
| SNPdbe | rs7963551 |
| MSV3d | rs7963551 |
| GWAS Ctlg | rs7963551 |
| GMAF | 0.1299 |
| Max Magnitude | 0 |
[PMID 23188672] Genetic variation in a hsa-let-7 binding site in RAD52 is associated with breast cancer susceptibility
[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.
[PMID 29024686] Increased age-adjusted hazard of death associated with a common single nucleotide polymorphism of the human RAD52 gene in a cardiovascular cohort.
