rs6764623
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6764623(A;A) |
| Make rs6764623(A;C) |
| Make rs6764623(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 1004354 |
| Gene | CNTN6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6764623 |
| dbSNP (classic) | rs6764623 |
| ClinGen | rs6764623 |
| ebi | rs6764623 |
| HLI | rs6764623 |
| Exac | rs6764623 |
| Gnomad | rs6764623 |
| Varsome | rs6764623 |
| LitVar | rs6764623 |
| Map | rs6764623 |
| PheGenI | rs6764623 |
| Biobank | rs6764623 |
| 1000 genomes | rs6764623 |
| hgdp | rs6764623 |
| ensembl | rs6764623 |
| geneview | rs6764623 |
| scholar | rs6764623 |
| rs6764623 | |
| pharmgkb | rs6764623 |
| gwascentral | rs6764623 |
| openSNP | rs6764623 |
| 23andMe | rs6764623 |
| SNPshot | rs6764623 |
| SNPdbe | rs6764623 |
| MSV3d | rs6764623 |
| GWAS Ctlg | rs6764623 |
| GMAF | 0.3329 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23650146 ]
|
| Trait | Venous thromboembolism |
| Title | A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. |
| Risk Allele | C |
| P-val | 2E-6 |
| Odds Ratio | 1.18 [1.10-1.26] |
