rs4844096
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4844096(A;A) |
| Make rs4844096(A;G) |
| Make rs4844096(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 69585474 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4844096 |
| dbSNP (classic) | rs4844096 |
| ClinGen | rs4844096 |
| ebi | rs4844096 |
| HLI | rs4844096 |
| Exac | rs4844096 |
| Gnomad | rs4844096 |
| Varsome | rs4844096 |
| LitVar | rs4844096 |
| Map | rs4844096 |
| PheGenI | rs4844096 |
| Biobank | rs4844096 |
| 1000 genomes | rs4844096 |
| hgdp | rs4844096 |
| ensembl | rs4844096 |
| geneview | rs4844096 |
| scholar | rs4844096 |
| rs4844096 | |
| pharmgkb | rs4844096 |
| gwascentral | rs4844096 |
| openSNP | rs4844096 |
| 23andMe | rs4844096 |
| SNPshot | rs4844096 |
| SNPdbe | rs4844096 |
| MSV3d | rs4844096 |
| GWAS Ctlg | rs4844096 |
| GMAF | 0.2267 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20195514 ]
|
| Trait | Primary tooth development (number of teeth) |
| Title | Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy |
| Risk Allele | G |
| P-val | 5E-11 |
| Odds Ratio | 0.73 [NR] % variance explained |
