rs771895449
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (AG;AG) | 0 | common in clinvar |
| Make rs771895449(-;-) |
| Make rs771895449(-;AG) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 8 |
| Position | 38145983 |
| Gene | STAR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs771895449 |
| dbSNP (classic) | rs771895449 |
| ClinGen | rs771895449 |
| ebi | rs771895449 |
| HLI | rs771895449 |
| Exac | rs771895449 |
| Gnomad | rs771895449 |
| Varsome | rs771895449 |
| LitVar | rs771895449 |
| Map | rs771895449 |
| PheGenI | rs771895449 |
| Biobank | rs771895449 |
| 1000 genomes | rs771895449 |
| hgdp | rs771895449 |
| ensembl | rs771895449 |
| geneview | rs771895449 |
| scholar | rs771895449 |
| rs771895449 | |
| pharmgkb | rs771895449 |
| gwascentral | rs771895449 |
| openSNP | rs771895449 |
| 23andMe | rs771895449 |
| SNPshot | rs771895449 |
| SNPdbe | rs771895449 |
| MSV3d | rs771895449 |
| GWAS Ctlg | rs771895449 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs771895449(-;-) |
| Alt | rs771895449(-;-) |
| Reference | Rs771895449(AG;AG) |
| Significance | Probable-Pathogenic |
| Disease | Cholesterol monooxygenase (side-chain cleaving) deficiency |
| Variation | info |
| Gene | STAR |
| CLNDBN | Cholesterol monooxygenase (side-chain cleaving) deficiency |
| Reversed | 0 |
| HGVS | NC_000008.10:g.38003501_38003502delAG |
| CLNSRC | |
| CLNACC | RCV000410363.1, |
