rs2071598
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2071598(A;A) |
| Make rs2071598(A;C) |
| Make rs2071598(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 98117279 |
| Gene | POP1, RIDA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2071598 |
| dbSNP (classic) | rs2071598 |
| ClinGen | rs2071598 |
| ebi | rs2071598 |
| HLI | rs2071598 |
| Exac | rs2071598 |
| Gnomad | rs2071598 |
| Varsome | rs2071598 |
| LitVar | rs2071598 |
| Map | rs2071598 |
| PheGenI | rs2071598 |
| Biobank | rs2071598 |
| 1000 genomes | rs2071598 |
| hgdp | rs2071598 |
| ensembl | rs2071598 |
| geneview | rs2071598 |
| scholar | rs2071598 |
| rs2071598 | |
| pharmgkb | rs2071598 |
| gwascentral | rs2071598 |
| openSNP | rs2071598 |
| 23andMe | rs2071598 |
| SNPshot | rs2071598 |
| SNPdbe | rs2071598 |
| MSV3d | rs2071598 |
| GWAS Ctlg | rs2071598 |
| GMAF | 0.1869 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22210626 ]
|
| Trait | |
| Title | Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. |
| Risk Allele | |
| P-val | 0.000009 |
| Odds Ratio | 1.2646 None |
