rs1959122
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common genotype |
| Make rs1959122(A;G) |
| Make rs1959122(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 14 |
| Position | 81871321 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1959122 |
| dbSNP (classic) | rs1959122 |
| ClinGen | rs1959122 |
| ebi | rs1959122 |
| HLI | rs1959122 |
| Exac | rs1959122 |
| Gnomad | rs1959122 |
| Varsome | rs1959122 |
| LitVar | rs1959122 |
| Map | rs1959122 |
| PheGenI | rs1959122 |
| Biobank | rs1959122 |
| 1000 genomes | rs1959122 |
| hgdp | rs1959122 |
| ensembl | rs1959122 |
| geneview | rs1959122 |
| scholar | rs1959122 |
| rs1959122 | |
| pharmgkb | rs1959122 |
| gwascentral | rs1959122 |
| openSNP | rs1959122 |
| 23andMe | rs1959122 |
| SNPshot | rs1959122 |
| SNPdbe | rs1959122 |
| MSV3d | rs1959122 |
| GWAS Ctlg | rs1959122 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | 9E-7 |
| Odds Ratio | 7.63 [2.92-19.95] |
