rs13088462
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 |
| Make rs13088462(C;C) |
| Make rs13088462(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 51034282 |
| Gene | DOCK3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13088462 |
| dbSNP (classic) | rs13088462 |
| ClinGen | rs13088462 |
| ebi | rs13088462 |
| HLI | rs13088462 |
| Exac | rs13088462 |
| Gnomad | rs13088462 |
| Varsome | rs13088462 |
| LitVar | rs13088462 |
| Map | rs13088462 |
| PheGenI | rs13088462 |
| Biobank | rs13088462 |
| 1000 genomes | rs13088462 |
| hgdp | rs13088462 |
| ensembl | rs13088462 |
| geneview | rs13088462 |
| scholar | rs13088462 |
| rs13088462 | |
| pharmgkb | rs13088462 |
| gwascentral | rs13088462 |
| openSNP | rs13088462 |
| 23andMe | rs13088462 |
| SNPshot | rs13088462 |
| SNPdbe | rs13088462 |
| MSV3d | rs13088462 |
| GWAS Ctlg | rs13088462 |
| GMAF | 0.01837 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | T |
| P-val | 4E-10 |
| Odds Ratio | 0.0500 [NR] meters decrease |
