rs10479002
From SNPedia
| Merged into | rs12777 |
| Orientation | plus |
| Stabilized | plus |
| Make rs10479002(C;C) |
| Make rs10479002(C;G) |
| Make rs10479002(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 132335969 |
| Gene | MIR4750, SLC22A4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10479002 |
| dbSNP (classic) | rs10479002 |
| ClinGen | rs10479002 |
| ebi | rs10479002 |
| HLI | rs10479002 |
| Exac | rs10479002 |
| Gnomad | rs10479002 |
| Varsome | rs10479002 |
| LitVar | rs10479002 |
| Map | rs10479002 |
| PheGenI | rs10479002 |
| Biobank | rs10479002 |
| 1000 genomes | rs10479002 |
| hgdp | rs10479002 |
| ensembl | rs10479002 |
| geneview | rs10479002 |
| scholar | rs10479002 |
| rs10479002 | |
| pharmgkb | rs10479002 |
| gwascentral | rs10479002 |
| openSNP | rs10479002 |
| 23andMe | rs10479002 |
| SNPshot | rs10479002 |
| SNPdbe | rs10479002 |
| MSV3d | rs10479002 |
| GWAS Ctlg | rs10479002 |
| Status | Merged into rs12777 |
| Max Magnitude | 0 |
| ? | (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 |
