rs11931532
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11931532(C;C) |
| Make rs11931532(C;T) |
| Make rs11931532(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 15724143 |
| Gene | BST1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11931532 |
| dbSNP (classic) | rs11931532 |
| ClinGen | rs11931532 |
| ebi | rs11931532 |
| HLI | rs11931532 |
| Exac | rs11931532 |
| Gnomad | rs11931532 |
| Varsome | rs11931532 |
| LitVar | rs11931532 |
| Map | rs11931532 |
| PheGenI | rs11931532 |
| Biobank | rs11931532 |
| 1000 genomes | rs11931532 |
| hgdp | rs11931532 |
| ensembl | rs11931532 |
| geneview | rs11931532 |
| scholar | rs11931532 |
| rs11931532 | |
| pharmgkb | rs11931532 |
| gwascentral | rs11931532 |
| openSNP | rs11931532 |
| 23andMe | rs11931532 |
| SNPshot | rs11931532 |
| SNPdbe | rs11931532 |
| MSV3d | rs11931532 |
| GWAS Ctlg | rs11931532 |
| GMAF | 0.2351 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23026536] Lack of association between BST1 polymorphisms and sporadic Parkinson's disease in a Japanese population
[PMID 20413655
] Genetics of neurodegenerative diseases: insights from high-throughput resequencing.
