rs1570106
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1570106(A;A) |
| Make rs1570106(A;G) |
| Make rs1570106(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 14 |
| Position | 68346398 |
| Gene | RAD51B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1570106 |
| dbSNP (classic) | rs1570106 |
| ClinGen | rs1570106 |
| ebi | rs1570106 |
| HLI | rs1570106 |
| Exac | rs1570106 |
| Gnomad | rs1570106 |
| Varsome | rs1570106 |
| LitVar | rs1570106 |
| Map | rs1570106 |
| PheGenI | rs1570106 |
| Biobank | rs1570106 |
| 1000 genomes | rs1570106 |
| hgdp | rs1570106 |
| ensembl | rs1570106 |
| geneview | rs1570106 |
| scholar | rs1570106 |
| rs1570106 | |
| pharmgkb | rs1570106 |
| gwascentral | rs1570106 |
| openSNP | rs1570106 |
| 23andMe | rs1570106 |
| SNPshot | rs1570106 |
| SNPdbe | rs1570106 |
| MSV3d | rs1570106 |
| GWAS Ctlg | rs1570106 |
| GMAF | 0.1217 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | T |
| P-val | 8E-9 |
| Odds Ratio | .03 [NR] unit decrease |
