rs3773364
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3773364(A;A) |
| Make rs3773364(A;G) |
| Make rs3773364(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 12148468 |
| Gene | SYN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3773364 |
| dbSNP (classic) | rs3773364 |
| ClinGen | rs3773364 |
| ebi | rs3773364 |
| HLI | rs3773364 |
| Exac | rs3773364 |
| Gnomad | rs3773364 |
| Varsome | rs3773364 |
| LitVar | rs3773364 |
| Map | rs3773364 |
| PheGenI | rs3773364 |
| Biobank | rs3773364 |
| 1000 genomes | rs3773364 |
| hgdp | rs3773364 |
| ensembl | rs3773364 |
| geneview | rs3773364 |
| scholar | rs3773364 |
| rs3773364 | |
| pharmgkb | rs3773364 |
| gwascentral | rs3773364 |
| openSNP | rs3773364 |
| 23andMe | rs3773364 |
| SNPshot | rs3773364 |
| SNPdbe | rs3773364 |
| MSV3d | rs3773364 |
| GWAS Ctlg | rs3773364 |
| GMAF | 0.2264 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20034013] Association of intronic polymorphism rs3773364 A>G in synapsin-2 gene with idiopathic epilepsy
[PMID 21465568] Lack of association between synapsin II (SYN2) gene polymorphism and susceptibility epilepsy: A case -control study and meta-analysis
