rs13058467
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs13058467(C;C) |
| Make rs13058467(C;T) |
| Make rs13058467(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 43183043 |
| Gene | TTLL12 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13058467 |
| dbSNP (classic) | rs13058467 |
| ClinGen | rs13058467 |
| ebi | rs13058467 |
| HLI | rs13058467 |
| Exac | rs13058467 |
| Gnomad | rs13058467 |
| Varsome | rs13058467 |
| LitVar | rs13058467 |
| Map | rs13058467 |
| PheGenI | rs13058467 |
| Biobank | rs13058467 |
| 1000 genomes | rs13058467 |
| hgdp | rs13058467 |
| ensembl | rs13058467 |
| geneview | rs13058467 |
| scholar | rs13058467 |
| rs13058467 | |
| pharmgkb | rs13058467 |
| gwascentral | rs13058467 |
| openSNP | rs13058467 |
| 23andMe | rs13058467 |
| SNPshot | rs13058467 |
| SNPdbe | rs13058467 |
| MSV3d | rs13058467 |
| GWAS Ctlg | rs13058467 |
| GMAF | 0.06061 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23918034] |
| Trait | Molar-incisor hypomineralization |
| Title | Genome-wide association study (GWAS) for molar-incisor hypomineralization (MIH). |
| Risk Allele | C |
| P-val | 4E-7 |
| Odds Ratio | 4.40 [2.5-7.8] |
