rs6500882
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6500882(G;G) |
| Make rs6500882(G;T) |
| Make rs6500882(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 6934780 |
| Gene | RBFOX1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6500882 |
| dbSNP (classic) | rs6500882 |
| ClinGen | rs6500882 |
| ebi | rs6500882 |
| HLI | rs6500882 |
| Exac | rs6500882 |
| Gnomad | rs6500882 |
| Varsome | rs6500882 |
| LitVar | rs6500882 |
| Map | rs6500882 |
| PheGenI | rs6500882 |
| Biobank | rs6500882 |
| 1000 genomes | rs6500882 |
| hgdp | rs6500882 |
| ensembl | rs6500882 |
| geneview | rs6500882 |
| scholar | rs6500882 |
| rs6500882 | |
| pharmgkb | rs6500882 |
| gwascentral | rs6500882 |
| openSNP | rs6500882 |
| 23andMe | rs6500882 |
| SNPshot | rs6500882 |
| SNPdbe | rs6500882 |
| MSV3d | rs6500882 |
| GWAS Ctlg | rs6500882 |
| GMAF | 0.3747 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19396477
] A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier?
