rs16861990
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 |
| Make rs16861990(A;C) |
| Make rs16861990(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 169165889 |
| Gene | NME7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16861990 |
| dbSNP (classic) | rs16861990 |
| ClinGen | rs16861990 |
| ebi | rs16861990 |
| HLI | rs16861990 |
| Exac | rs16861990 |
| Gnomad | rs16861990 |
| Varsome | rs16861990 |
| LitVar | rs16861990 |
| Map | rs16861990 |
| PheGenI | rs16861990 |
| Biobank | rs16861990 |
| 1000 genomes | rs16861990 |
| hgdp | rs16861990 |
| ensembl | rs16861990 |
| geneview | rs16861990 |
| scholar | rs16861990 |
| rs16861990 | |
| pharmgkb | rs16861990 |
| gwascentral | rs16861990 |
| openSNP | rs16861990 |
| 23andMe | rs16861990 |
| SNPshot | rs16861990 |
| SNPdbe | rs16861990 |
| MSV3d | rs16861990 |
| GWAS Ctlg | rs16861990 |
| GMAF | 0.05005 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21502573 ]
|
| Trait | |
| Title | Genetic predictors of fibrin D-dimer levels in healthy adults. |
| Risk Allele | C |
| P-val | 0.000002 |
| Odds Ratio | 0.0614 [NR] % increase |
| GWAS snp | |
|---|---|
| PMID | [PMID 22672568]
|
| Trait | |
| Title | A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q. |
| Risk Allele | C |
| P-val | 2E-12 |
| Odds Ratio | 2.0200 None |
