rs774528745
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs774528745(C;T) |
| Make rs774528745(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 2 |
| Position | 222221368 |
| Gene | LOC105373901, LOC107985991, PAX3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs774528745 |
| dbSNP (classic) | rs774528745 |
| ClinGen | rs774528745 |
| ebi | rs774528745 |
| HLI | rs774528745 |
| Exac | rs774528745 |
| Gnomad | rs774528745 |
| Varsome | rs774528745 |
| LitVar | rs774528745 |
| Map | rs774528745 |
| PheGenI | rs774528745 |
| Biobank | rs774528745 |
| 1000 genomes | rs774528745 |
| hgdp | rs774528745 |
| ensembl | rs774528745 |
| geneview | rs774528745 |
| scholar | rs774528745 |
| rs774528745 | |
| pharmgkb | rs774528745 |
| gwascentral | rs774528745 |
| openSNP | rs774528745 |
| 23andMe | rs774528745 |
| SNPshot | rs774528745 |
| SNPdbe | rs774528745 |
| MSV3d | rs774528745 |
| GWAS Ctlg | rs774528745 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs774528745(T;T) |
| Alt | rs774528745(T;T) |
| Reference | Rs774528745(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | PAX3 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.223086087C>T |
| CLNSRC | |
| CLNACC | RCV000372931.1, |
