rs2288073
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2288073(A;A) |
| Make rs2288073(A;G) |
| Make rs2288073(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 24190429 |
| Gene | FAM228A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2288073 |
| dbSNP (classic) | rs2288073 |
| ClinGen | rs2288073 |
| ebi | rs2288073 |
| HLI | rs2288073 |
| Exac | rs2288073 |
| Gnomad | rs2288073 |
| Varsome | rs2288073 |
| LitVar | rs2288073 |
| Map | rs2288073 |
| PheGenI | rs2288073 |
| Biobank | rs2288073 |
| 1000 genomes | rs2288073 |
| hgdp | rs2288073 |
| ensembl | rs2288073 |
| geneview | rs2288073 |
| scholar | rs2288073 |
| rs2288073 | |
| pharmgkb | rs2288073 |
| gwascentral | rs2288073 |
| openSNP | rs2288073 |
| 23andMe | rs2288073 |
| SNPshot | rs2288073 |
| SNPdbe | rs2288073 |
| MSV3d | rs2288073 |
| GWAS Ctlg | rs2288073 |
| GMAF | 0.2149 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23509962 ]
|
| Trait | Venous thromboembolism (gene x gene interaction) |
| Title | A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis. |
| Risk Allele | T |
| P-val | 2E-9 |
| Odds Ratio | 1.60 [NR] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 2
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
