rs39861
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs39861(C;C) |
| Make rs39861(C;T) |
| Make rs39861(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 66856430 |
| Gene | MAST4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs39861 |
| dbSNP (classic) | rs39861 |
| ClinGen | rs39861 |
| ebi | rs39861 |
| HLI | rs39861 |
| Exac | rs39861 |
| Gnomad | rs39861 |
| Varsome | rs39861 |
| LitVar | rs39861 |
| Map | rs39861 |
| PheGenI | rs39861 |
| Biobank | rs39861 |
| 1000 genomes | rs39861 |
| hgdp | rs39861 |
| ensembl | rs39861 |
| geneview | rs39861 |
| scholar | rs39861 |
| rs39861 | |
| pharmgkb | rs39861 |
| gwascentral | rs39861 |
| openSNP | rs39861 |
| 23andMe | rs39861 |
| SNPshot | rs39861 |
| SNPdbe | rs39861 |
| MSV3d | rs39861 |
| GWAS Ctlg | rs39861 |
| GMAF | 0.2755 |
| 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 | 3E-7 |
| Odds Ratio | 1.26 [1.13-1.41] |
