Rs1122794
From SNPedia
| Orientation | minus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1122794 |
| PheGenI | rs1122794 |
| nextbio | rs1122794 |
| hapmap | rs1122794 |
| 1000 genomes | rs1122794 |
| hgdp | rs1122794 |
| ensembl | rs1122794 |
| gopubmed | rs1122794 |
| geneview | rs1122794 |
| scholar | rs1122794 |
| rs1122794 | |
| pharmgkb | rs1122794 |
| gwascentral | rs1122794 |
| openSNP | rs1122794 |
| 23andMe | rs1122794 |
| 23andMe all | rs1122794 |
| SNP Nexus | |
| SNPshot | rs1122794 |
| SNPdbe | rs1122794 |
| MSV3d | rs1122794 |
| Gene | ITFG3 |
| Chromosome | 16 |
| Orientation | minus |
| GMAF | 0.1731 |
| Position | 309155 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs1122794(G;G) |
| Make rs1122794(G;T) |
| Make rs1122794(T;T) |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
| GWAS snp | |
|---|---|
| PMID | [PMID 19862010] |
| Trait | Mean corpuscular hemoglobin |
| Title | Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium |
| Risk Allele | A |
| P-val | 3E-10 |
| Odds Ratio | 0 [0.003-0.006] pg increase |
| GET Evidence | |
|---|---|
| rs1122794 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.210938 |
| summary | |
