rs12186641
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12186641(C;C) |
| Make rs12186641(C;T) |
| Make rs12186641(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 51868281 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12186641 |
| dbSNP (classic) | rs12186641 |
| ClinGen | rs12186641 |
| ebi | rs12186641 |
| HLI | rs12186641 |
| Exac | rs12186641 |
| Gnomad | rs12186641 |
| Varsome | rs12186641 |
| LitVar | rs12186641 |
| Map | rs12186641 |
| PheGenI | rs12186641 |
| Biobank | rs12186641 |
| 1000 genomes | rs12186641 |
| hgdp | rs12186641 |
| ensembl | rs12186641 |
| geneview | rs12186641 |
| scholar | rs12186641 |
| rs12186641 | |
| pharmgkb | rs12186641 |
| gwascentral | rs12186641 |
| openSNP | rs12186641 |
| 23andMe | rs12186641 |
| SNPshot | rs12186641 |
| SNPdbe | rs12186641 |
| MSV3d | rs12186641 |
| GWAS Ctlg | rs12186641 |
| GMAF | 0.04132 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23708191 ]
|
| Trait | Congenital heart disease |
| Title | Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16. |
| Risk Allele | |
| P-val | 7E-6 |
| Odds Ratio | 1.68 [NR] |
