rs3110496
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3110496(A;A) |
| Make rs3110496(A;G) |
| Make rs3110496(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 29590753 |
| Gene | ANKRD13B, GIT1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3110496 |
| dbSNP (classic) | rs3110496 |
| ClinGen | rs3110496 |
| ebi | rs3110496 |
| HLI | rs3110496 |
| Exac | rs3110496 |
| Gnomad | rs3110496 |
| Varsome | rs3110496 |
| LitVar | rs3110496 |
| Map | rs3110496 |
| PheGenI | rs3110496 |
| Biobank | rs3110496 |
| 1000 genomes | rs3110496 |
| hgdp | rs3110496 |
| ensembl | rs3110496 |
| geneview | rs3110496 |
| scholar | rs3110496 |
| rs3110496 | |
| pharmgkb | rs3110496 |
| gwascentral | rs3110496 |
| openSNP | rs3110496 |
| 23andMe | rs3110496 |
| SNPshot | rs3110496 |
| SNPdbe | rs3110496 |
| MSV3d | rs3110496 |
| GWAS Ctlg | rs3110496 |
| GMAF | 0.3118 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | A |
| P-val | 7E-9 |
| Odds Ratio | 0.0200 [NR] meters decrease |
