rs771121666
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs771121666(C;C) |
| Make rs771121666(C;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 22 |
| Position | 40365030 |
| Gene | ADSL |
| is a | snp |
| is | mentioned by |
| dbSNP | rs771121666 |
| dbSNP (classic) | rs771121666 |
| ClinGen | rs771121666 |
| ebi | rs771121666 |
| HLI | rs771121666 |
| Exac | rs771121666 |
| Gnomad | rs771121666 |
| Varsome | rs771121666 |
| LitVar | rs771121666 |
| Map | rs771121666 |
| PheGenI | rs771121666 |
| Biobank | rs771121666 |
| 1000 genomes | rs771121666 |
| hgdp | rs771121666 |
| ensembl | rs771121666 |
| geneview | rs771121666 |
| scholar | rs771121666 |
| rs771121666 | |
| pharmgkb | rs771121666 |
| gwascentral | rs771121666 |
| openSNP | rs771121666 |
| 23andMe | rs771121666 |
| SNPshot | rs771121666 |
| SNPdbe | rs771121666 |
| MSV3d | rs771121666 |
| GWAS Ctlg | rs771121666 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs771121666(C;C) |
| Alt | rs771121666(C;C) |
| Reference | Rs771121666(T;T) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ADSL |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000022.10:g.40761034T>C |
| CLNSRC | |
| CLNACC | RCV000224729.1, |
