rs2638953
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2638953(C;C) |
| Make rs2638953(C;G) |
| Make rs2638953(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 28381482 |
| Gene | CCDC91 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2638953 |
| dbSNP (classic) | rs2638953 |
| ClinGen | rs2638953 |
| ebi | rs2638953 |
| HLI | rs2638953 |
| Exac | rs2638953 |
| Gnomad | rs2638953 |
| Varsome | rs2638953 |
| LitVar | rs2638953 |
| Map | rs2638953 |
| PheGenI | rs2638953 |
| Biobank | rs2638953 |
| 1000 genomes | rs2638953 |
| hgdp | rs2638953 |
| ensembl | rs2638953 |
| geneview | rs2638953 |
| scholar | rs2638953 |
| rs2638953 | |
| pharmgkb | rs2638953 |
| gwascentral | rs2638953 |
| openSNP | rs2638953 |
| 23andMe | rs2638953 |
| SNPshot | rs2638953 |
| SNPdbe | rs2638953 |
| MSV3d | rs2638953 |
| GWAS Ctlg | rs2638953 |
| GMAF | 0.2456 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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 | C |
| P-val | 7E-17 |
| Odds Ratio | 0.03 [NR] unit increase |
