rs4366490
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4366490(C;C) |
| Make rs4366490(C;T) |
| Make rs4366490(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 11 |
| Position | 63145382 |
| Gene | SLC22A24 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4366490 |
| dbSNP (classic) | rs4366490 |
| ClinGen | rs4366490 |
| ebi | rs4366490 |
| HLI | rs4366490 |
| Exac | rs4366490 |
| Gnomad | rs4366490 |
| Varsome | rs4366490 |
| LitVar | rs4366490 |
| Map | rs4366490 |
| PheGenI | rs4366490 |
| Biobank | rs4366490 |
| 1000 genomes | rs4366490 |
| hgdp | rs4366490 |
| ensembl | rs4366490 |
| geneview | rs4366490 |
| scholar | rs4366490 |
| rs4366490 | |
| pharmgkb | rs4366490 |
| gwascentral | rs4366490 |
| openSNP | rs4366490 |
| 23andMe | rs4366490 |
| SNPshot | rs4366490 |
| SNPdbe | rs4366490 |
| MSV3d | rs4366490 |
| GWAS Ctlg | rs4366490 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24800985 ]
|
| Trait | Conotruncal heart defects |
| Title | Genome-wide association study of maternal and inherited loci for conotruncal heart defects. |
| Risk Allele | |
| P-val | 1E-6 |
| Odds Ratio | 1.70 [1.36-2.12] |
