rs1799922
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1799922(A;A) |
| Make rs1799922(A;C) |
| Make rs1799922(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 128775141 |
| Gene | OPN1SW |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1799922 |
| dbSNP (classic) | rs1799922 |
| ClinGen | rs1799922 |
| ebi | rs1799922 |
| HLI | rs1799922 |
| Exac | rs1799922 |
| Gnomad | rs1799922 |
| Varsome | rs1799922 |
| LitVar | rs1799922 |
| Map | rs1799922 |
| PheGenI | rs1799922 |
| Biobank | rs1799922 |
| 1000 genomes | rs1799922 |
| hgdp | rs1799922 |
| ensembl | rs1799922 |
| geneview | rs1799922 |
| scholar | rs1799922 |
| rs1799922 | |
| pharmgkb | rs1799922 |
| gwascentral | rs1799922 |
| openSNP | rs1799922 |
| 23andMe | rs1799922 |
| SNPshot | rs1799922 |
| SNPdbe | rs1799922 |
| MSV3d | rs1799922 |
| GWAS Ctlg | rs1799922 |
| GMAF | 0.2309 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23704328 ]
|
| Trait | Primary tooth development (number of teeth) |
| Title | Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances. |
| Risk Allele | T |
| P-val | 4E-9 |
| Odds Ratio | .14 [0.097-0.191] unit increase |
