rs8079702
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8079702(A;A) |
| Make rs8079702(A;G) |
| Make rs8079702(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 70194685 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8079702 |
| dbSNP (classic) | rs8079702 |
| ClinGen | rs8079702 |
| ebi | rs8079702 |
| HLI | rs8079702 |
| Exac | rs8079702 |
| Gnomad | rs8079702 |
| Varsome | rs8079702 |
| LitVar | rs8079702 |
| Map | rs8079702 |
| PheGenI | rs8079702 |
| Biobank | rs8079702 |
| 1000 genomes | rs8079702 |
| hgdp | rs8079702 |
| ensembl | rs8079702 |
| geneview | rs8079702 |
| scholar | rs8079702 |
| rs8079702 | |
| pharmgkb | rs8079702 |
| gwascentral | rs8079702 |
| openSNP | rs8079702 |
| 23andMe | rs8079702 |
| SNPshot | rs8079702 |
| SNPdbe | rs8079702 |
| MSV3d | rs8079702 |
| GWAS Ctlg | rs8079702 |
| GMAF | 0.478 |
| 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 | 1E-14 |
| Odds Ratio | 1.15 [NR] % variance explained |
[PMID 31270966] The research of ion channel-related gene polymorphisms with atrial fibrillation in the Chinese Han population.
