rs412000
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs412000(C;C) |
| Make rs412000(C;G) |
| Make rs412000(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 58631697 |
| Gene | LOC105371842, TEX14 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs412000 |
| dbSNP (classic) | rs412000 |
| ClinGen | rs412000 |
| ebi | rs412000 |
| HLI | rs412000 |
| Exac | rs412000 |
| Gnomad | rs412000 |
| Varsome | rs412000 |
| LitVar | rs412000 |
| Map | rs412000 |
| PheGenI | rs412000 |
| Biobank | rs412000 |
| 1000 genomes | rs412000 |
| hgdp | rs412000 |
| ensembl | rs412000 |
| geneview | rs412000 |
| scholar | rs412000 |
| rs412000 | |
| pharmgkb | rs412000 |
| gwascentral | rs412000 |
| openSNP | rs412000 |
| 23andMe | rs412000 |
| SNPshot | rs412000 |
| SNPdbe | rs412000 |
| MSV3d | rs412000 |
| GWAS Ctlg | rs412000 |
| GMAF | 0.4082 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23704328 ]
|
| Trait | Primary tooth development (time to first tooth eruption) |
| Title | Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances. |
| Risk Allele | C |
| P-val | 2E-9 |
| Odds Ratio | .16 [0.11-0.22] unit decrease |
