rs5936487
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs5936487(A;A) |
| Make rs5936487(A;G) |
| Make rs5936487(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 69673072 |
| Gene | EDA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5936487 |
| dbSNP (classic) | rs5936487 |
| ClinGen | rs5936487 |
| ebi | rs5936487 |
| HLI | rs5936487 |
| Exac | rs5936487 |
| Gnomad | rs5936487 |
| Varsome | rs5936487 |
| LitVar | rs5936487 |
| Map | rs5936487 |
| PheGenI | rs5936487 |
| Biobank | rs5936487 |
| 1000 genomes | rs5936487 |
| hgdp | rs5936487 |
| ensembl | rs5936487 |
| geneview | rs5936487 |
| scholar | rs5936487 |
| rs5936487 | |
| pharmgkb | rs5936487 |
| gwascentral | rs5936487 |
| openSNP | rs5936487 |
| 23andMe | rs5936487 |
| SNPshot | rs5936487 |
| SNPdbe | rs5936487 |
| MSV3d | rs5936487 |
| GWAS Ctlg | rs5936487 |
| GMAF | 0.2497 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20195514 ]
|
| Trait | Primary tooth development (time to first tooth eruption) |
| Title | Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy |
| Risk Allele | G |
| P-val | 6E-11 |
| Odds Ratio | 0.50 [NR] % variance explained |
