rs149610079
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 3 | Carrier of mutation predisposing to brainstem viral encephalitis |
| (G;G) | 0 | common/normal |
| Make rs149610079(A;A) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 3 |
| Position | 138167206 |
| Gene | DBR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs149610079 |
| dbSNP (classic) | rs149610079 |
| ClinGen | rs149610079 |
| ebi | rs149610079 |
| HLI | rs149610079 |
| Exac | rs149610079 |
| Gnomad | rs149610079 |
| Varsome | rs149610079 |
| LitVar | rs149610079 |
| Map | rs149610079 |
| PheGenI | rs149610079 |
| Biobank | rs149610079 |
| 1000 genomes | rs149610079 |
| hgdp | rs149610079 |
| ensembl | rs149610079 |
| geneview | rs149610079 |
| scholar | rs149610079 |
| rs149610079 | |
| pharmgkb | rs149610079 |
| gwascentral | rs149610079 |
| openSNP | rs149610079 |
| 23andMe | rs149610079 |
| SNPshot | rs149610079 |
| SNPdbe | rs149610079 |
| MSV3d | rs149610079 |
| GWAS Ctlg | rs149610079 |
| Max Magnitude | 3 |
aka c.589C>T (p.R197X)
Mutation in DBR1 gene pathogenic for predisposition to brainstem viral encephalitis (when inherited recessively); [PMID 29474921
]
