rs2237060
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2237060(A;A) |
| Make rs2237060(A;C) |
| Make rs2237060(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 132635193 |
| Gene | RAD50, TH2LCRR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2237060 |
| dbSNP (classic) | rs2237060 |
| ClinGen | rs2237060 |
| ebi | rs2237060 |
| HLI | rs2237060 |
| Exac | rs2237060 |
| Gnomad | rs2237060 |
| Varsome | rs2237060 |
| LitVar | rs2237060 |
| Map | rs2237060 |
| PheGenI | rs2237060 |
| Biobank | rs2237060 |
| 1000 genomes | rs2237060 |
| hgdp | rs2237060 |
| ensembl | rs2237060 |
| geneview | rs2237060 |
| scholar | rs2237060 |
| rs2237060 | |
| pharmgkb | rs2237060 |
| gwascentral | rs2237060 |
| openSNP | rs2237060 |
| 23andMe | rs2237060 |
| SNPshot | rs2237060 |
| SNPdbe | rs2237060 |
| MSV3d | rs2237060 |
| GWAS Ctlg | rs2237060 |
| GMAF | 0.2176 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
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| ||
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[PMID 20805886] Unique DNA repair gene variations and potential associations with the primary antibody deficiency syndromes IgAD and CVID.
