rs999905
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs999905(C;C) |
| Make rs999905(C;G) |
| Make rs999905(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 88020640 |
| Gene | NTRK3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs999905 |
| dbSNP (classic) | rs999905 |
| ClinGen | rs999905 |
| ebi | rs999905 |
| HLI | rs999905 |
| Exac | rs999905 |
| Gnomad | rs999905 |
| Varsome | rs999905 |
| LitVar | rs999905 |
| Map | rs999905 |
| PheGenI | rs999905 |
| Biobank | rs999905 |
| 1000 genomes | rs999905 |
| hgdp | rs999905 |
| ensembl | rs999905 |
| geneview | rs999905 |
| scholar | rs999905 |
| rs999905 | |
| pharmgkb | rs999905 |
| gwascentral | rs999905 |
| openSNP | rs999905 |
| 23andMe | rs999905 |
| SNPshot | rs999905 |
| SNPdbe | rs999905 |
| MSV3d | rs999905 |
| GWAS Ctlg | rs999905 |
| GMAF | 0.2681 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19344762] Evidence for a possible association of neurotrophin receptor (NTRK-3) gene polymorphisms with hippocampal function and schizophrenia
