rs1896312
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1896312(A;A) |
| Make rs1896312(A;G) |
| Make rs1896312(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 114908619 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1896312 |
| dbSNP (classic) | rs1896312 |
| ClinGen | rs1896312 |
| ebi | rs1896312 |
| HLI | rs1896312 |
| Exac | rs1896312 |
| Gnomad | rs1896312 |
| Varsome | rs1896312 |
| LitVar | rs1896312 |
| Map | rs1896312 |
| PheGenI | rs1896312 |
| Biobank | rs1896312 |
| 1000 genomes | rs1896312 |
| hgdp | rs1896312 |
| ensembl | rs1896312 |
| geneview | rs1896312 |
| scholar | rs1896312 |
| rs1896312 | |
| pharmgkb | rs1896312 |
| gwascentral | rs1896312 |
| openSNP | rs1896312 |
| 23andMe | rs1896312 |
| SNPshot | rs1896312 |
| SNPdbe | rs1896312 |
| MSV3d | rs1896312 |
| GWAS Ctlg | rs1896312 |
| GMAF | 0.3664 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20062060 ]
|
| Trait | PR interval |
| Title | Genome-wide association study of PR interval |
| Risk Allele | C |
| P-val | 3E-17 |
| Odds Ratio | 1.95 [1.50-2.40] ms increase |
[PMID 21347284] Genome-wide association studies of the PR interval in African Americans.
