rs141446687
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 7.7 | X-linked adrenoleukodystrophy; symptoms and age of onset highly variable |
| (A;C) | 4.4 | Carrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possible |
| (C;C) | 0 | common/normal |
| Make rs141446687(C;G) |
| Make rs141446687(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | X |
| Position | 153737191 |
| Gene | ABCD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs141446687 |
| dbSNP (classic) | rs141446687 |
| ClinGen | rs141446687 |
| ebi | rs141446687 |
| HLI | rs141446687 |
| Exac | rs141446687 |
| Gnomad | rs141446687 |
| Varsome | rs141446687 |
| LitVar | rs141446687 |
| Map | rs141446687 |
| PheGenI | rs141446687 |
| Biobank | rs141446687 |
| 1000 genomes | rs141446687 |
| hgdp | rs141446687 |
| ensembl | rs141446687 |
| geneview | rs141446687 |
| scholar | rs141446687 |
| rs141446687 | |
| pharmgkb | rs141446687 |
| gwascentral | rs141446687 |
| openSNP | rs141446687 |
| 23andMe | rs141446687 |
| SNPshot | rs141446687 |
| SNPdbe | rs141446687 |
| MSV3d | rs141446687 |
| GWAS Ctlg | rs141446687 |
| Max Magnitude | 7.7 |
