rs683250
From SNPedia
| Orientation | plus |
| Make rs683250(A;A) |
| Make rs683250(A;G) |
| Make rs683250(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 11 |
| Position | 83565125 |
| Gene | DLG2, LOC107984425 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs683250 |
| dbSNP (classic) | rs683250 |
| ClinGen | rs683250 |
| ebi | rs683250 |
| HLI | rs683250 |
| Exac | rs683250 |
| Gnomad | rs683250 |
| Varsome | rs683250 |
| LitVar | rs683250 |
| Map | rs683250 |
| PheGenI | rs683250 |
| Biobank | rs683250 |
| 1000 genomes | rs683250 |
| hgdp | rs683250 |
| ensembl | rs683250 |
| geneview | rs683250 |
| scholar | rs683250 |
| rs683250 | |
| pharmgkb | rs683250 |
| gwascentral | rs683250 |
| openSNP | rs683250 |
| 23andMe | rs683250 |
| SNPshot | rs683250 |
| SNPdbe | rs683250 |
| MSV3d | rs683250 |
| GWAS Ctlg | rs683250 |
| Max Magnitude | 0 |
[PMID 30699873
] Concordance of genetic variation that increases risk for anxiety disorders and posttraumatic stress disorders and that influences their underlying neurocircuitry.
