rs778947880
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs778947880(C;T) |
| Make rs778947880(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 18 |
| Position | 21765807 |
| Gene | MIB1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs778947880 |
| dbSNP (classic) | rs778947880 |
| ClinGen | rs778947880 |
| ebi | rs778947880 |
| HLI | rs778947880 |
| Exac | rs778947880 |
| Gnomad | rs778947880 |
| Varsome | rs778947880 |
| LitVar | rs778947880 |
| Map | rs778947880 |
| PheGenI | rs778947880 |
| Biobank | rs778947880 |
| 1000 genomes | rs778947880 |
| hgdp | rs778947880 |
| ensembl | rs778947880 |
| geneview | rs778947880 |
| scholar | rs778947880 |
| rs778947880 | |
| pharmgkb | rs778947880 |
| gwascentral | rs778947880 |
| openSNP | rs778947880 |
| 23andMe | rs778947880 |
| SNPshot | rs778947880 |
| SNPdbe | rs778947880 |
| MSV3d | rs778947880 |
| GWAS Ctlg | rs778947880 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs778947880(G;G) rs778947880(T;T) |
| Alt | rs778947880(G;G) rs778947880(T;T) |
| Reference | Rs778947880(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | MIB1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000018.9:g.19345768C>T |
| CLNSRC | |
| CLNACC | RCV000481876.1, |
