rs1890397
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1890397(A;A) |
Make rs1890397(A;G) |
Make rs1890397(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 192801803 |
is a | snp |
is | mentioned by |
dbSNP | rs1890397 |
dbSNP (classic) | rs1890397 |
ClinGen | rs1890397 |
ebi | rs1890397 |
HLI | rs1890397 |
Exac | rs1890397 |
Gnomad | rs1890397 |
Varsome | rs1890397 |
LitVar | rs1890397 |
Map | rs1890397 |
PheGenI | rs1890397 |
Biobank | rs1890397 |
1000 genomes | rs1890397 |
hgdp | rs1890397 |
ensembl | rs1890397 |
geneview | rs1890397 |
scholar | rs1890397 |
rs1890397 | |
pharmgkb | rs1890397 |
gwascentral | rs1890397 |
openSNP | rs1890397 |
23andMe | rs1890397 |
SNPshot | rs1890397 |
SNPdbe | rs1890397 |
MSV3d | rs1890397 |
GWAS Ctlg | rs1890397 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25740197] RGS2 ggenetic variation: Association analysis with panic disorder and dimensional as well as intermediate phenotypes of anxiety