rs295301
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs295301(A;A) |
| Make rs295301(A;G) |
| Make rs295301(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 141619799 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs295301 |
| dbSNP (classic) | rs295301 |
| ClinGen | rs295301 |
| ebi | rs295301 |
| HLI | rs295301 |
| Exac | rs295301 |
| Gnomad | rs295301 |
| Varsome | rs295301 |
| LitVar | rs295301 |
| Map | rs295301 |
| PheGenI | rs295301 |
| Biobank | rs295301 |
| 1000 genomes | rs295301 |
| hgdp | rs295301 |
| ensembl | rs295301 |
| geneview | rs295301 |
| scholar | rs295301 |
| rs295301 | |
| pharmgkb | rs295301 |
| gwascentral | rs295301 |
| openSNP | rs295301 |
| 23andMe | rs295301 |
| SNPshot | rs295301 |
| SNPdbe | rs295301 |
| MSV3d | rs295301 |
| GWAS Ctlg | rs295301 |
| GMAF | 0.3866 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22210626
] Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP
