rs36098294
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs36098294(C;T) |
| Make rs36098294(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 87227421 |
| Gene | CHMP2B, MIR4795 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs36098294 |
| dbSNP (classic) | rs36098294 |
| ClinGen | rs36098294 |
| ebi | rs36098294 |
| HLI | rs36098294 |
| Exac | rs36098294 |
| Gnomad | rs36098294 |
| Varsome | rs36098294 |
| LitVar | rs36098294 |
| Map | rs36098294 |
| PheGenI | rs36098294 |
| Biobank | rs36098294 |
| 1000 genomes | rs36098294 |
| hgdp | rs36098294 |
| ensembl | rs36098294 |
| geneview | rs36098294 |
| scholar | rs36098294 |
| rs36098294 | |
| pharmgkb | rs36098294 |
| gwascentral | rs36098294 |
| openSNP | rs36098294 |
| 23andMe | rs36098294 |
| SNPshot | rs36098294 |
| SNPdbe | rs36098294 |
| MSV3d | rs36098294 |
| GWAS Ctlg | rs36098294 |
| GMAF | 0.004591 |
| Max Magnitude | 0 |
[PMID 20412296] Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients
| ClinVar | |
|---|---|
| Risk | rs36098294(T;T) |
| Alt | rs36098294(T;T) |
| Reference | Rs36098294(C;C) |
| Significance | Probable-non-pathogenic |
| Disease | Frontotemporal dementia |
| Variation | info |
| Gene | CHMP2B MIR4795 |
| CLNDBN | Frontotemporal dementia |
| Reversed | 0 |
| HGVS | NC_000003.11:g.87276571C>T |
| CLNSRC | |
| CLNACC | RCV000286148.1, |
