rs9373124
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9373124(C;C) |
| Make rs9373124(C;T) |
| Make rs9373124(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 135102071 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9373124 |
| dbSNP (classic) | rs9373124 |
| ClinGen | rs9373124 |
| ebi | rs9373124 |
| HLI | rs9373124 |
| Exac | rs9373124 |
| Gnomad | rs9373124 |
| Varsome | rs9373124 |
| LitVar | rs9373124 |
| Map | rs9373124 |
| PheGenI | rs9373124 |
| Biobank | rs9373124 |
| 1000 genomes | rs9373124 |
| hgdp | rs9373124 |
| ensembl | rs9373124 |
| geneview | rs9373124 |
| scholar | rs9373124 |
| rs9373124 | |
| pharmgkb | rs9373124 |
| gwascentral | rs9373124 |
| openSNP | rs9373124 |
| 23andMe | rs9373124 |
| SNPshot | rs9373124 |
| SNPdbe | rs9373124 |
| MSV3d | rs9373124 |
| GWAS Ctlg | rs9373124 |
| GMAF | 0.3356 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19862010 ]
|
| Trait | Other erythrocyte phenotypes |
| Title | Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium |
| Risk Allele | C |
| P-val | 7E-14 |
| Odds Ratio | 0 [0.002-0.003] g/dl decrease |
| GWAS snp | |
|---|---|
| PMID | [PMID 21738478]
|
| Trait | |
| Title | Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. |
| Risk Allele | T |
| P-val | 1E-10 |
| Odds Ratio | 0.0800 [0.06-0.10] unit increase |
