rs2486001
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2486001(A;A) |
Make rs2486001(A;G) |
Make rs2486001(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 44010315 |
Gene | SLC6A9 |
is a | snp |
is | mentioned by |
dbSNP | rs2486001 |
dbSNP (classic) | rs2486001 |
ClinGen | rs2486001 |
ebi | rs2486001 |
HLI | rs2486001 |
Exac | rs2486001 |
Gnomad | rs2486001 |
Varsome | rs2486001 |
LitVar | rs2486001 |
Map | rs2486001 |
PheGenI | rs2486001 |
Biobank | rs2486001 |
1000 genomes | rs2486001 |
hgdp | rs2486001 |
ensembl | rs2486001 |
geneview | rs2486001 |
scholar | rs2486001 |
rs2486001 | |
pharmgkb | rs2486001 |
gwascentral | rs2486001 |
openSNP | rs2486001 |
23andMe | rs2486001 |
SNPshot | rs2486001 |
SNPdbe | rs2486001 |
MSV3d | rs2486001 |
GWAS Ctlg | rs2486001 |
GMAF | 0.1524 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 17582620] significant association with methamphetamine dependence among a sample of 204 assumedly Japanese patients with methamphetamine-use disorder and 210 controls. a haplotype consisting of rs2486001(T)-rs2248829(C) was noted as being a significant risk factor (OR = 2.04, p = 0.000039)
[PMID 19556729] Association of SLC6A9 Gene Variants with Human Essential Hypertension