rs776720591
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs776720591(A;G) |
| Make rs776720591(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 22 |
| Position | 37755099 |
| Gene | TRIOBP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs776720591 |
| dbSNP (classic) | rs776720591 |
| ClinGen | rs776720591 |
| ebi | rs776720591 |
| HLI | rs776720591 |
| Exac | rs776720591 |
| Gnomad | rs776720591 |
| Varsome | rs776720591 |
| LitVar | rs776720591 |
| Map | rs776720591 |
| PheGenI | rs776720591 |
| Biobank | rs776720591 |
| 1000 genomes | rs776720591 |
| hgdp | rs776720591 |
| ensembl | rs776720591 |
| geneview | rs776720591 |
| scholar | rs776720591 |
| rs776720591 | |
| pharmgkb | rs776720591 |
| gwascentral | rs776720591 |
| openSNP | rs776720591 |
| 23andMe | rs776720591 |
| SNPshot | rs776720591 |
| SNPdbe | rs776720591 |
| MSV3d | rs776720591 |
| GWAS Ctlg | rs776720591 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs776720591(G;G) |
| Alt | rs776720591(G;G) |
| Reference | Rs776720591(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | TRIOBP |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000022.10:g.38151106A>G |
| CLNSRC | |
| CLNACC | RCV000480502.1, |
