rs1048771
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1048771(C;C) |
| Make rs1048771(C;T) |
| Make rs1048771(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 46278228 |
| Gene | LRRC41, RAD54L |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1048771 |
| dbSNP (classic) | rs1048771 |
| ClinGen | rs1048771 |
| ebi | rs1048771 |
| HLI | rs1048771 |
| Exac | rs1048771 |
| Gnomad | rs1048771 |
| Varsome | rs1048771 |
| LitVar | rs1048771 |
| Map | rs1048771 |
| PheGenI | rs1048771 |
| Biobank | rs1048771 |
| 1000 genomes | rs1048771 |
| hgdp | rs1048771 |
| ensembl | rs1048771 |
| geneview | rs1048771 |
| scholar | rs1048771 |
| rs1048771 | |
| pharmgkb | rs1048771 |
| gwascentral | rs1048771 |
| openSNP | rs1048771 |
| 23andMe | rs1048771 |
| SNPshot | rs1048771 |
| SNPdbe | rs1048771 |
| MSV3d | rs1048771 |
| GWAS Ctlg | rs1048771 |
| GMAF | 0.1455 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 26514363] Genetic variations in the homologous recombination repair pathway genes modify risk of glioma
