rs1048456
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1048456(A;A) |
| Make rs1048456(A;C) |
| Make rs1048456(C;C) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 5 |
| Position | 141641152 |
| Gene | FCHSD1, RELL2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1048456 |
| dbSNP (classic) | rs1048456 |
| ClinGen | rs1048456 |
| ebi | rs1048456 |
| HLI | rs1048456 |
| Exac | rs1048456 |
| Gnomad | rs1048456 |
| Varsome | rs1048456 |
| LitVar | rs1048456 |
| Map | rs1048456 |
| PheGenI | rs1048456 |
| Biobank | rs1048456 |
| 1000 genomes | rs1048456 |
| hgdp | rs1048456 |
| ensembl | rs1048456 |
| geneview | rs1048456 |
| scholar | rs1048456 |
| rs1048456 | |
| pharmgkb | rs1048456 |
| gwascentral | rs1048456 |
| openSNP | rs1048456 |
| 23andMe | rs1048456 |
| SNPshot | rs1048456 |
| SNPdbe | rs1048456 |
| MSV3d | rs1048456 |
| GWAS Ctlg | rs1048456 |
| Max Magnitude | 0 |
[PMID 24707947] Genetic markers in a multi-ethnic sample for childhood acute lymphoblastic leukemia risk
