rs12694997
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12694997(A;A) |
| Make rs12694997(A;G) |
| Make rs12694997(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 241323571 |
| Gene | SEPT2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12694997 |
| dbSNP (classic) | rs12694997 |
| ClinGen | rs12694997 |
| ebi | rs12694997 |
| HLI | rs12694997 |
| Exac | rs12694997 |
| Gnomad | rs12694997 |
| Varsome | rs12694997 |
| LitVar | rs12694997 |
| Map | rs12694997 |
| PheGenI | rs12694997 |
| Biobank | rs12694997 |
| 1000 genomes | rs12694997 |
| hgdp | rs12694997 |
| ensembl | rs12694997 |
| geneview | rs12694997 |
| scholar | rs12694997 |
| rs12694997 | |
| pharmgkb | rs12694997 |
| gwascentral | rs12694997 |
| openSNP | rs12694997 |
| 23andMe | rs12694997 |
| SNPshot | rs12694997 |
| SNPdbe | rs12694997 |
| MSV3d | rs12694997 |
| GWAS Ctlg | rs12694997 |
| GMAF | 0.1497 |
| 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 | A |
| P-val | 1E-8 |
| Odds Ratio | .02 [NR] unit decrease |
