rs1019670
From SNPedia
| Merged into | rs7232 |
| Orientation | plus |
| Stabilized | plus |
| Make rs1019670(A;A) |
| Make rs1019670(A;T) |
| Make rs1019670(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 11 |
| Position | 60173126 |
| Gene | MS4A6A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1019670 |
| dbSNP (classic) | rs1019670 |
| ClinGen | rs1019670 |
| ebi | rs1019670 |
| HLI | rs1019670 |
| Exac | rs1019670 |
| Gnomad | rs1019670 |
| Varsome | rs1019670 |
| LitVar | rs1019670 |
| Map | rs1019670 |
| PheGenI | rs1019670 |
| Biobank | rs1019670 |
| 1000 genomes | rs1019670 |
| hgdp | rs1019670 |
| ensembl | rs1019670 |
| geneview | rs1019670 |
| scholar | rs1019670 |
| rs1019670 | |
| pharmgkb | rs1019670 |
| gwascentral | rs1019670 |
| openSNP | rs1019670 |
| 23andMe | rs1019670 |
| SNPshot | rs1019670 |
| SNPdbe | rs1019670 |
| MSV3d | rs1019670 |
| GWAS Ctlg | rs1019670 |
| Status | Merged into rs7232 |
| Max Magnitude | 0 |
| 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 | 4E-9 |
| Odds Ratio | .01 [0.005-0.009] unit decrease |
