rs72823592
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs72823592(A;A) |
| Make rs72823592(A;G) |
| Make rs72823592(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 48045642 |
| Gene | COPZ2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs72823592 |
| dbSNP (classic) | rs72823592 |
| ClinGen | rs72823592 |
| ebi | rs72823592 |
| HLI | rs72823592 |
| Exac | rs72823592 |
| Gnomad | rs72823592 |
| Varsome | rs72823592 |
| LitVar | rs72823592 |
| Map | rs72823592 |
| PheGenI | rs72823592 |
| Biobank | rs72823592 |
| 1000 genomes | rs72823592 |
| hgdp | rs72823592 |
| ensembl | rs72823592 |
| geneview | rs72823592 |
| scholar | rs72823592 |
| rs72823592 | |
| pharmgkb | rs72823592 |
| gwascentral | rs72823592 |
| openSNP | rs72823592 |
| 23andMe | rs72823592 |
| SNPshot | rs72823592 |
| SNPdbe | rs72823592 |
| MSV3d | rs72823592 |
| GWAS Ctlg | rs72823592 |
| GMAF | 0.129 |
| Max Magnitude | 0 |
| 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 | G |
| P-val | 9E-9 |
| Odds Ratio | 1.30 [1.20-1.41] |
