rs1126179
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1126179(C;C) |
| Make rs1126179(C;T) |
| Make rs1126179(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 65861461 |
| Gene | LOC101927676 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1126179 |
| dbSNP (classic) | rs1126179 |
| ClinGen | rs1126179 |
| ebi | rs1126179 |
| HLI | rs1126179 |
| Exac | rs1126179 |
| Gnomad | rs1126179 |
| Varsome | rs1126179 |
| LitVar | rs1126179 |
| Map | rs1126179 |
| PheGenI | rs1126179 |
| Biobank | rs1126179 |
| 1000 genomes | rs1126179 |
| hgdp | rs1126179 |
| ensembl | rs1126179 |
| geneview | rs1126179 |
| scholar | rs1126179 |
| rs1126179 | |
| pharmgkb | rs1126179 |
| gwascentral | rs1126179 |
| openSNP | rs1126179 |
| 23andMe | rs1126179 |
| SNPshot | rs1126179 |
| SNPdbe | rs1126179 |
| MSV3d | rs1126179 |
| GWAS Ctlg | rs1126179 |
| GMAF | 0.3641 |
| 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 | G |
| P-val | 3E-6 |
| Odds Ratio | 2.13 [1.55-2.92] |
