rs488333
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs488333(A;A) |
| Make rs488333(A;G) |
| Make rs488333(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 84281955 |
| Gene | SEMA3A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs488333 |
| dbSNP (classic) | rs488333 |
| ClinGen | rs488333 |
| ebi | rs488333 |
| HLI | rs488333 |
| Exac | rs488333 |
| Gnomad | rs488333 |
| Varsome | rs488333 |
| LitVar | rs488333 |
| Map | rs488333 |
| PheGenI | rs488333 |
| Biobank | rs488333 |
| 1000 genomes | rs488333 |
| hgdp | rs488333 |
| ensembl | rs488333 |
| geneview | rs488333 |
| scholar | rs488333 |
| rs488333 | |
| pharmgkb | rs488333 |
| gwascentral | rs488333 |
| openSNP | rs488333 |
| 23andMe | rs488333 |
| SNPshot | rs488333 |
| SNPdbe | rs488333 |
| MSV3d | rs488333 |
| GWAS Ctlg | rs488333 |
| GMAF | 0.2397 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | 0.000003 |
| Odds Ratio | 1.2681 None |
