rs11242111
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11242111(A;A) |
| Make rs11242111(A;G) |
| Make rs11242111(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 5 |
| Position | 132420366 |
| Gene | C5orf56, LOC102723741 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11242111 |
| dbSNP (classic) | rs11242111 |
| ClinGen | rs11242111 |
| ebi | rs11242111 |
| HLI | rs11242111 |
| Exac | rs11242111 |
| Gnomad | rs11242111 |
| Varsome | rs11242111 |
| LitVar | rs11242111 |
| Map | rs11242111 |
| PheGenI | rs11242111 |
| Biobank | rs11242111 |
| 1000 genomes | rs11242111 |
| hgdp | rs11242111 |
| ensembl | rs11242111 |
| geneview | rs11242111 |
| scholar | rs11242111 |
| rs11242111 | |
| pharmgkb | rs11242111 |
| gwascentral | rs11242111 |
| openSNP | rs11242111 |
| 23andMe | rs11242111 |
| SNPshot | rs11242111 |
| SNPdbe | rs11242111 |
| MSV3d | rs11242111 |
| GWAS Ctlg | rs11242111 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23969696 ]
|
| Trait | Fibrinogen |
| Title | Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. |
| Risk Allele | A |
| P-val | 2E-21 |
| Odds Ratio | .02 [0.019-0.027] unit increase |
