rs773726323
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs773726323(C;T) |
| Make rs773726323(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 2 |
| Position | 189062882 |
| Gene | COL5A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs773726323 |
| dbSNP (classic) | rs773726323 |
| ClinGen | rs773726323 |
| ebi | rs773726323 |
| HLI | rs773726323 |
| Exac | rs773726323 |
| Gnomad | rs773726323 |
| Varsome | rs773726323 |
| LitVar | rs773726323 |
| Map | rs773726323 |
| PheGenI | rs773726323 |
| Biobank | rs773726323 |
| 1000 genomes | rs773726323 |
| hgdp | rs773726323 |
| ensembl | rs773726323 |
| geneview | rs773726323 |
| scholar | rs773726323 |
| rs773726323 | |
| pharmgkb | rs773726323 |
| gwascentral | rs773726323 |
| openSNP | rs773726323 |
| 23andMe | rs773726323 |
| SNPshot | rs773726323 |
| SNPdbe | rs773726323 |
| MSV3d | rs773726323 |
| GWAS Ctlg | rs773726323 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs773726323(T;T) |
| Alt | rs773726323(T;T) |
| Reference | Rs773726323(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | COL5A2 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.189927608C>T |
| CLNSRC | |
| CLNACC | RCV000200772.1, |
