rs3744165
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3744165(A;A) |
| Make rs3744165(A;C) |
| Make rs3744165(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 82832566 |
| Gene | TBCD, ZNF750 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3744165 |
| dbSNP (classic) | rs3744165 |
| ClinGen | rs3744165 |
| ebi | rs3744165 |
| HLI | rs3744165 |
| Exac | rs3744165 |
| Gnomad | rs3744165 |
| Varsome | rs3744165 |
| LitVar | rs3744165 |
| Map | rs3744165 |
| PheGenI | rs3744165 |
| Biobank | rs3744165 |
| 1000 genomes | rs3744165 |
| hgdp | rs3744165 |
| ensembl | rs3744165 |
| geneview | rs3744165 |
| scholar | rs3744165 |
| rs3744165 | |
| pharmgkb | rs3744165 |
| gwascentral | rs3744165 |
| openSNP | rs3744165 |
| 23andMe | rs3744165 |
| SNPshot | rs3744165 |
| SNPdbe | rs3744165 |
| MSV3d | rs3744165 |
| GWAS Ctlg | rs3744165 |
| GMAF | 0.1625 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 26728569] Common variants on 17q25 and gene-gene interactions conferring risk of schizophrenia in Han Chinese population and regulating gene expressions in human brain.
