rs547918064
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs547918064(C;C) |
| Make rs547918064(C;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 15 |
| Position | 100898147 |
| Gene | ALDH1A3, LOC101927751 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs547918064 |
| dbSNP (classic) | rs547918064 |
| ClinGen | rs547918064 |
| ebi | rs547918064 |
| HLI | rs547918064 |
| Exac | rs547918064 |
| Gnomad | rs547918064 |
| Varsome | rs547918064 |
| LitVar | rs547918064 |
| Map | rs547918064 |
| PheGenI | rs547918064 |
| Biobank | rs547918064 |
| 1000 genomes | rs547918064 |
| hgdp | rs547918064 |
| ensembl | rs547918064 |
| geneview | rs547918064 |
| scholar | rs547918064 |
| rs547918064 | |
| pharmgkb | rs547918064 |
| gwascentral | rs547918064 |
| openSNP | rs547918064 |
| 23andMe | rs547918064 |
| SNPshot | rs547918064 |
| SNPdbe | rs547918064 |
| MSV3d | rs547918064 |
| GWAS Ctlg | rs547918064 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs547918064(C;C) rs547918064(T;T) |
| Alt | rs547918064(C;C) rs547918064(T;T) |
| Reference | Rs547918064(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | LOC101927751 ALDH1A3 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000015.9:g.101438352G>A |
| CLNSRC | |
| CLNACC | RCV000493670.1, |
