rs1122794
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1122794(G;G) |
| Make rs1122794(G;T) |
| Make rs1122794(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 259156 |
| Gene | FAM234A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1122794 |
| dbSNP (classic) | rs1122794 |
| ClinGen | rs1122794 |
| ebi | rs1122794 |
| HLI | rs1122794 |
| Exac | rs1122794 |
| Gnomad | rs1122794 |
| Varsome | rs1122794 |
| LitVar | rs1122794 |
| Map | rs1122794 |
| PheGenI | rs1122794 |
| Biobank | rs1122794 |
| 1000 genomes | rs1122794 |
| hgdp | rs1122794 |
| ensembl | rs1122794 |
| geneview | rs1122794 |
| scholar | rs1122794 |
| rs1122794 | |
| pharmgkb | rs1122794 |
| gwascentral | rs1122794 |
| openSNP | rs1122794 |
| 23andMe | rs1122794 |
| SNPshot | rs1122794 |
| SNPdbe | rs1122794 |
| MSV3d | rs1122794 |
| GWAS Ctlg | rs1122794 |
| GMAF | 0.1726 |
| Max Magnitude | 0 |
| ? | (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 |
| GWAS snp | |
|---|---|
| PMID | [PMID 23446634]
|
| Trait | Red blood cell traits |
| Title | Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network. |
| Risk Allele | A |
| P-val | 7E-6 |
| Odds Ratio | .23 [0.13-0.33] pg increase |
