rs8077696
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs8077696(A;A) |
| Make rs8077696(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 65196443 |
| Gene | RGS9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8077696 |
| dbSNP (classic) | rs8077696 |
| ClinGen | rs8077696 |
| ebi | rs8077696 |
| HLI | rs8077696 |
| Exac | rs8077696 |
| Gnomad | rs8077696 |
| Varsome | rs8077696 |
| LitVar | rs8077696 |
| Map | rs8077696 |
| PheGenI | rs8077696 |
| Biobank | rs8077696 |
| 1000 genomes | rs8077696 |
| hgdp | rs8077696 |
| ensembl | rs8077696 |
| geneview | rs8077696 |
| scholar | rs8077696 |
| rs8077696 | |
| pharmgkb | rs8077696 |
| gwascentral | rs8077696 |
| openSNP | rs8077696 |
| 23andMe | rs8077696 |
| SNPshot | rs8077696 |
| SNPdbe | rs8077696 |
| MSV3d | rs8077696 |
| GWAS Ctlg | rs8077696 |
| GMAF | 0.2534 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 18548510] Analysis of genetic variations in the RGS9 gene and antipsychotic-induced tardive dyskinesia in schizophrenia.
