rs12799172
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12799172(C;C) |
| Make rs12799172(C;T) |
| Make rs12799172(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 6728826 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12799172 |
| dbSNP (classic) | rs12799172 |
| ClinGen | rs12799172 |
| ebi | rs12799172 |
| HLI | rs12799172 |
| Exac | rs12799172 |
| Gnomad | rs12799172 |
| Varsome | rs12799172 |
| LitVar | rs12799172 |
| Map | rs12799172 |
| PheGenI | rs12799172 |
| Biobank | rs12799172 |
| 1000 genomes | rs12799172 |
| hgdp | rs12799172 |
| ensembl | rs12799172 |
| geneview | rs12799172 |
| scholar | rs12799172 |
| rs12799172 | |
| pharmgkb | rs12799172 |
| gwascentral | rs12799172 |
| openSNP | rs12799172 |
| 23andMe | rs12799172 |
| SNPshot | rs12799172 |
| SNPdbe | rs12799172 |
| MSV3d | rs12799172 |
| GWAS Ctlg | rs12799172 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24347629 ]
|
| Trait | Periodontal disease-related phenotypes |
| Title | Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years. |
| Risk Allele | |
| P-val | 5E-6 |
| Odds Ratio | 2.12 [NR] |
