rs10770705
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10770705(A;A) |
| Make rs10770705(A;C) |
| Make rs10770705(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 20704533 |
| Gene | SLCO1C1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10770705 |
| dbSNP (classic) | rs10770705 |
| ClinGen | rs10770705 |
| ebi | rs10770705 |
| HLI | rs10770705 |
| Exac | rs10770705 |
| Gnomad | rs10770705 |
| Varsome | rs10770705 |
| LitVar | rs10770705 |
| Map | rs10770705 |
| PheGenI | rs10770705 |
| Biobank | rs10770705 |
| 1000 genomes | rs10770705 |
| hgdp | rs10770705 |
| ensembl | rs10770705 |
| geneview | rs10770705 |
| scholar | rs10770705 |
| rs10770705 | |
| pharmgkb | rs10770705 |
| gwascentral | rs10770705 |
| openSNP | rs10770705 |
| 23andMe | rs10770705 |
| SNPshot | rs10770705 |
| SNPdbe | rs10770705 |
| MSV3d | rs10770705 |
| GWAS Ctlg | rs10770705 |
| GMAF | 0.2713 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height |
| Risk Allele | A |
| P-val | 8E-18 |
| Odds Ratio | 0.03 [NR] unit increase |
