rs17105278
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17105278(C;C) |
| Make rs17105278(C;T) |
| Make rs17105278(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 68261762 |
| Gene | RAD51B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17105278 |
| dbSNP (classic) | rs17105278 |
| ClinGen | rs17105278 |
| ebi | rs17105278 |
| HLI | rs17105278 |
| Exac | rs17105278 |
| Gnomad | rs17105278 |
| Varsome | rs17105278 |
| LitVar | rs17105278 |
| Map | rs17105278 |
| PheGenI | rs17105278 |
| Biobank | rs17105278 |
| 1000 genomes | rs17105278 |
| hgdp | rs17105278 |
| ensembl | rs17105278 |
| geneview | rs17105278 |
| scholar | rs17105278 |
| rs17105278 | |
| pharmgkb | rs17105278 |
| gwascentral | rs17105278 |
| openSNP | rs17105278 |
| 23andMe | rs17105278 |
| SNPshot | rs17105278 |
| SNPdbe | rs17105278 |
| MSV3d | rs17105278 |
| GWAS Ctlg | rs17105278 |
| GMAF | 0.303 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 24526414
] In-depth analyses unveil the association and possible functional involvement of novel RAD51B polymorphisms in age-related macular degeneration
[PMID 29024686] Increased age-adjusted hazard of death associated with a common single nucleotide polymorphism of the human RAD52 gene in a cardiovascular cohort.
