rs6499100
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6499100(C;C) |
| Make rs6499100(C;T) |
| Make rs6499100(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 52797550 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6499100 |
| dbSNP (classic) | rs6499100 |
| ClinGen | rs6499100 |
| ebi | rs6499100 |
| HLI | rs6499100 |
| Exac | rs6499100 |
| Gnomad | rs6499100 |
| Varsome | rs6499100 |
| LitVar | rs6499100 |
| Map | rs6499100 |
| PheGenI | rs6499100 |
| Biobank | rs6499100 |
| 1000 genomes | rs6499100 |
| hgdp | rs6499100 |
| ensembl | rs6499100 |
| geneview | rs6499100 |
| scholar | rs6499100 |
| rs6499100 | |
| pharmgkb | rs6499100 |
| gwascentral | rs6499100 |
| openSNP | rs6499100 |
| 23andMe | rs6499100 |
| SNPshot | rs6499100 |
| SNPdbe | rs6499100 |
| MSV3d | rs6499100 |
| GWAS Ctlg | rs6499100 |
| GMAF | 0.4729 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23297363 ]
|
| Trait | Tetralogy of Fallot |
| Title | Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot. |
| Risk Allele | A |
| P-val | 1E-6 |
| Odds Ratio | 1.26 [1.14-1.4] |
