rs71651682
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs71651682(C;T) |
| Make rs71651682(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 26772759 |
| Gene | GABRB3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs71651682 |
| dbSNP (classic) | rs71651682 |
| ClinGen | rs71651682 |
| ebi | rs71651682 |
| HLI | rs71651682 |
| Exac | rs71651682 |
| Gnomad | rs71651682 |
| Varsome | rs71651682 |
| LitVar | rs71651682 |
| Map | rs71651682 |
| PheGenI | rs71651682 |
| Biobank | rs71651682 |
| 1000 genomes | rs71651682 |
| hgdp | rs71651682 |
| ensembl | rs71651682 |
| geneview | rs71651682 |
| scholar | rs71651682 |
| rs71651682 | |
| pharmgkb | rs71651682 |
| gwascentral | rs71651682 |
| openSNP | rs71651682 |
| 23andMe | rs71651682 |
| SNPshot | rs71651682 |
| SNPdbe | rs71651682 |
| MSV3d | rs71651682 |
| GWAS Ctlg | rs71651682 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs71651682(T;T) |
| Alt | rs71651682(T;T) |
| Reference | Rs71651682(C;C) |
| Significance | Other |
| Disease | Epilepsy |
| Variation | info |
| Gene | GABRB3 |
| CLNDBN | Epilepsy, childhood absence 5 |
| Reversed | 0 |
| HGVS | NC_000015.9:g.27017906C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000017577.3, |
