rs2075671
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2075671(C;C) |
| Make rs2075671(C;T) |
| Make rs2075671(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 100747483 |
| Gene | ZAN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2075671 |
| dbSNP (classic) | rs2075671 |
| ClinGen | rs2075671 |
| ebi | rs2075671 |
| HLI | rs2075671 |
| Exac | rs2075671 |
| Gnomad | rs2075671 |
| Varsome | rs2075671 |
| LitVar | rs2075671 |
| Map | rs2075671 |
| PheGenI | rs2075671 |
| Biobank | rs2075671 |
| 1000 genomes | rs2075671 |
| hgdp | rs2075671 |
| ensembl | rs2075671 |
| geneview | rs2075671 |
| scholar | rs2075671 |
| rs2075671 | |
| pharmgkb | rs2075671 |
| gwascentral | rs2075671 |
| openSNP | rs2075671 |
| 23andMe | rs2075671 |
| SNPshot | rs2075671 |
| SNPdbe | rs2075671 |
| MSV3d | rs2075671 |
| GWAS Ctlg | rs2075671 |
| GMAF | 0.1648 |
| 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 | A |
| P-val | 1E-9 |
| Odds Ratio | 0 [0.005-0.009] 1 M cell/mm^3 increase |
