Rs10479002
From SNPedia
| Merged into | rs12777 |
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10479002 |
| PheGenI | rs10479002 |
| nextbio | rs10479002 |
| hapmap | rs10479002 |
| 1000 genomes | rs10479002 |
| hgdp | rs10479002 |
| ensembl | rs10479002 |
| gopubmed | rs10479002 |
| geneview | rs10479002 |
| scholar | rs10479002 |
| rs10479002 | |
| pharmgkb | rs10479002 |
| gwascentral | rs10479002 |
| openSNP | rs10479002 |
| 23andMe | rs10479002 |
| 23andMe all | rs10479002 |
| SNP Nexus | |
| SNPshot | rs10479002 |
| SNPdbe | rs10479002 |
| MSV3d | rs10479002 |
| Status | Merged into rs12777 |
| Gene | MIR4750, SLC22A4 |
| Chromosome | 5 |
| Orientation | plus |
| Position | 131671662 |
| Reference | GRCh37.p5 37.3/137 |
| Max Magnitude |
| Make rs10479002(C;C) |
| Make rs10479002(C;G) |
| Make rs10479002(G;G) |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
| GWAS snp | |
|---|---|
| PMID | [PMID 20031577] |
| Trait | Fibrinogen |
| Title | Novel Loci, Including Those Related to Crohn Disease, Psoriasis, and Inflammation Identified in a Genome-Wide Association Study of Fibrinogen in 17,686 Women: The Women's Genome Health Study |
| Risk Allele | C |
| P-val | 0.000001 |
| Odds Ratio | 9.51 [NR] mg/dl increase |
