rs764831063
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common/normal |
| Make rs764831063(A;G) |
| Make rs764831063(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 1 |
| Position | 26447535 |
| Gene | DHDDS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs764831063 |
| dbSNP (classic) | rs764831063 |
| ClinGen | rs764831063 |
| ebi | rs764831063 |
| HLI | rs764831063 |
| Exac | rs764831063 |
| Gnomad | rs764831063 |
| Varsome | rs764831063 |
| LitVar | rs764831063 |
| Map | rs764831063 |
| PheGenI | rs764831063 |
| Biobank | rs764831063 |
| 1000 genomes | rs764831063 |
| hgdp | rs764831063 |
| ensembl | rs764831063 |
| geneview | rs764831063 |
| scholar | rs764831063 |
| rs764831063 | |
| pharmgkb | rs764831063 |
| gwascentral | rs764831063 |
| openSNP | rs764831063 |
| 23andMe | rs764831063 |
| SNPshot | rs764831063 |
| SNPdbe | rs764831063 |
| MSV3d | rs764831063 |
| GWAS Ctlg | rs764831063 |
| Max Magnitude | 0 |
Non-coding variant assessed as part of Blueprint Genetics Retinal dystrophy (266 gene) panel.
