rs10831234
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10831234(C;C) |
| Make rs10831234(C;T) |
| Make rs10831234(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 11 |
| Position | 94500021 |
| Gene | ANKRD49, MRE11A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10831234 |
| dbSNP (classic) | rs10831234 |
| ClinGen | rs10831234 |
| ebi | rs10831234 |
| HLI | rs10831234 |
| Exac | rs10831234 |
| Gnomad | rs10831234 |
| Varsome | rs10831234 |
| LitVar | rs10831234 |
| Map | rs10831234 |
| PheGenI | rs10831234 |
| Biobank | rs10831234 |
| 1000 genomes | rs10831234 |
| hgdp | rs10831234 |
| ensembl | rs10831234 |
| geneview | rs10831234 |
| scholar | rs10831234 |
| rs10831234 | |
| pharmgkb | rs10831234 |
| gwascentral | rs10831234 |
| openSNP | rs10831234 |
| 23andMe | rs10831234 |
| SNPshot | rs10831234 |
| SNPdbe | rs10831234 |
| MSV3d | rs10831234 |
| GWAS Ctlg | rs10831234 |
| Max Magnitude | 0 |
[PMID 26514363] Genetic variations in the homologous recombination repair pathway genes modify risk of glioma
