rs34976462
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs34976462(C;G) |
| Make rs34976462(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 87600893 |
| Gene | ABCB1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34976462 |
| dbSNP (classic) | rs34976462 |
| ClinGen | rs34976462 |
| ebi | rs34976462 |
| HLI | rs34976462 |
| Exac | rs34976462 |
| Gnomad | rs34976462 |
| Varsome | rs34976462 |
| LitVar | rs34976462 |
| Map | rs34976462 |
| PheGenI | rs34976462 |
| Biobank | rs34976462 |
| 1000 genomes | rs34976462 |
| hgdp | rs34976462 |
| ensembl | rs34976462 |
| geneview | rs34976462 |
| scholar | rs34976462 |
| rs34976462 | |
| pharmgkb | rs34976462 |
| gwascentral | rs34976462 |
| openSNP | rs34976462 |
| 23andMe | rs34976462 |
| SNPshot | rs34976462 |
| SNPdbe | rs34976462 |
| MSV3d | rs34976462 |
| GWAS Ctlg | rs34976462 |
| GMAF | 0.002296 |
| Max Magnitude | 0 |
[PMID 24572589] Novel and functional ABCB1 gene variant in sporadic Parkinson's disease
