rs771390
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs771390(C;C) |
| Make rs771390(C;T) |
| Make rs771390(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 34285335 |
| Gene | LOC105378639 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs771390 |
| dbSNP (classic) | rs771390 |
| ClinGen | rs771390 |
| ebi | rs771390 |
| HLI | rs771390 |
| Exac | rs771390 |
| Gnomad | rs771390 |
| Varsome | rs771390 |
| LitVar | rs771390 |
| Map | rs771390 |
| PheGenI | rs771390 |
| Biobank | rs771390 |
| 1000 genomes | rs771390 |
| hgdp | rs771390 |
| ensembl | rs771390 |
| geneview | rs771390 |
| scholar | rs771390 |
| rs771390 | |
| pharmgkb | rs771390 |
| gwascentral | rs771390 |
| openSNP | rs771390 |
| 23andMe | rs771390 |
| SNPshot | rs771390 |
| SNPdbe | rs771390 |
| MSV3d | rs771390 |
| GWAS Ctlg | rs771390 |
| GMAF | 0.1648 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22949513] |
| Trait | Epilepsy (generalized) |
| Title | Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 |
| Risk Allele | C |
| P-val | 6E-7 |
| Odds Ratio | 1.22 [1.12-1.32] |
