rs769931291
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs769931291(C;T) |
| Make rs769931291(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 5 |
| Position | 150376328 |
| Gene | TCOF1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs769931291 |
| dbSNP (classic) | rs769931291 |
| ClinGen | rs769931291 |
| ebi | rs769931291 |
| HLI | rs769931291 |
| Exac | rs769931291 |
| Gnomad | rs769931291 |
| Varsome | rs769931291 |
| LitVar | rs769931291 |
| Map | rs769931291 |
| PheGenI | rs769931291 |
| Biobank | rs769931291 |
| 1000 genomes | rs769931291 |
| hgdp | rs769931291 |
| ensembl | rs769931291 |
| geneview | rs769931291 |
| scholar | rs769931291 |
| rs769931291 | |
| pharmgkb | rs769931291 |
| gwascentral | rs769931291 |
| openSNP | rs769931291 |
| 23andMe | rs769931291 |
| SNPshot | rs769931291 |
| SNPdbe | rs769931291 |
| MSV3d | rs769931291 |
| GWAS Ctlg | rs769931291 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs769931291(G;G) rs769931291(T;T) |
| Alt | rs769931291(G;G) rs769931291(T;T) |
| Reference | Rs769931291(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | TCOF1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000005.9:g.149755891C>T |
| CLNSRC | |
| CLNACC | RCV000480820.1, |
