rs596359
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs596359(A;A) |
Make rs596359(A;G) |
Make rs596359(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 6 |
Position | 153135918 |
is a | snp |
is | mentioned by |
dbSNP | rs596359 |
dbSNP (classic) | rs596359 |
ClinGen | rs596359 |
ebi | rs596359 |
HLI | rs596359 |
Exac | rs596359 |
Gnomad | rs596359 |
Varsome | rs596359 |
LitVar | rs596359 |
Map | rs596359 |
PheGenI | rs596359 |
Biobank | rs596359 |
1000 genomes | rs596359 |
hgdp | rs596359 |
ensembl | rs596359 |
geneview | rs596359 |
scholar | rs596359 |
rs596359 | |
pharmgkb | rs596359 |
gwascentral | rs596359 |
openSNP | rs596359 |
23andMe | rs596359 |
SNPshot | rs596359 |
SNPdbe | rs596359 |
MSV3d | rs596359 |
GWAS Ctlg | rs596359 |
GMAF | 0.4674 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22591552] Variation in regulator of G-Protein signaling 17 Gene (RGS17) is associated with multiple substance dependence diagnoses