rs2292593
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs2292593(A;G) |
Make rs2292593(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 65201802 |
Gene | RGS9 |
is a | snp |
is | mentioned by |
dbSNP | rs2292593 |
dbSNP (classic) | rs2292593 |
ClinGen | rs2292593 |
ebi | rs2292593 |
HLI | rs2292593 |
Exac | rs2292593 |
Gnomad | rs2292593 |
Varsome | rs2292593 |
LitVar | rs2292593 |
Map | rs2292593 |
PheGenI | rs2292593 |
Biobank | rs2292593 |
1000 genomes | rs2292593 |
hgdp | rs2292593 |
ensembl | rs2292593 |
geneview | rs2292593 |
scholar | rs2292593 |
rs2292593 | |
pharmgkb | rs2292593 |
gwascentral | rs2292593 |
openSNP | rs2292593 |
23andMe | rs2292593 |
SNPshot | rs2292593 |
SNPdbe | rs2292593 |
MSV3d | rs2292593 |
GWAS Ctlg | rs2292593 |
GMAF | 0.2603 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 18548510] Analysis of genetic variations in the RGS9 gene and antipsychotic-induced tardive dyskinesia in schizophrenia.