rs2474937
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2474937(C;C) |
| Make rs2474937(C;T) |
| Make rs2474937(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 118360355 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2474937 |
| dbSNP (classic) | rs2474937 |
| ClinGen | rs2474937 |
| ebi | rs2474937 |
| HLI | rs2474937 |
| Exac | rs2474937 |
| Gnomad | rs2474937 |
| Varsome | rs2474937 |
| LitVar | rs2474937 |
| Map | rs2474937 |
| PheGenI | rs2474937 |
| Biobank | rs2474937 |
| 1000 genomes | rs2474937 |
| hgdp | rs2474937 |
| ensembl | rs2474937 |
| geneview | rs2474937 |
| scholar | rs2474937 |
| rs2474937 | |
| pharmgkb | rs2474937 |
| gwascentral | rs2474937 |
| openSNP | rs2474937 |
| 23andMe | rs2474937 |
| SNPshot | rs2474937 |
| SNPdbe | rs2474937 |
| MSV3d | rs2474937 |
| GWAS Ctlg | rs2474937 |
| GMAF | 0.2107 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23708190] |
| Trait | Congenital heart malformation |
| Title | A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations. |
| Risk Allele | C |
| P-val | 8E-10 |
| Odds Ratio | 1.40 [1.26-1.56] |
[PMID 25875170
] Association between the European GWAS-Identified Susceptibility Locus at Chromosome 4p16 and the Risk of Atrial Septal Defect: A Case-Control Study in Southwest China and a Meta-Analysis
