rs3729639
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs3729639(C;T) |
| Make rs3729639(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 67191598 |
| Gene | E2F4, EXOC3L1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3729639 |
| dbSNP (classic) | rs3729639 |
| ClinGen | rs3729639 |
| ebi | rs3729639 |
| HLI | rs3729639 |
| Exac | rs3729639 |
| Gnomad | rs3729639 |
| Varsome | rs3729639 |
| LitVar | rs3729639 |
| Map | rs3729639 |
| PheGenI | rs3729639 |
| Biobank | rs3729639 |
| 1000 genomes | rs3729639 |
| hgdp | rs3729639 |
| ensembl | rs3729639 |
| geneview | rs3729639 |
| scholar | rs3729639 |
| rs3729639 | |
| pharmgkb | rs3729639 |
| gwascentral | rs3729639 |
| openSNP | rs3729639 |
| 23andMe | rs3729639 |
| SNPshot | rs3729639 |
| SNPdbe | rs3729639 |
| MSV3d | rs3729639 |
| GWAS Ctlg | rs3729639 |
| GMAF | 0.152 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21347282 ]
|
| Trait | |
| Title | Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project |
| Risk Allele | T |
| P-val | 2E-11 |
| Odds Ratio | 0.0900 [0.06-0.12] SD increase |
