rs2279709
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2279709(G;G) |
Make rs2279709(G;T) |
Make rs2279709(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 8 |
Position | 20178722 |
Gene | SLC18A1 |
is a | snp |
is | mentioned by |
dbSNP | rs2279709 |
dbSNP (classic) | rs2279709 |
ClinGen | rs2279709 |
ebi | rs2279709 |
HLI | rs2279709 |
Exac | rs2279709 |
Gnomad | rs2279709 |
Varsome | rs2279709 |
LitVar | rs2279709 |
Map | rs2279709 |
PheGenI | rs2279709 |
Biobank | rs2279709 |
1000 genomes | rs2279709 |
hgdp | rs2279709 |
ensembl | rs2279709 |
geneview | rs2279709 |
scholar | rs2279709 |
rs2279709 | |
pharmgkb | rs2279709 |
gwascentral | rs2279709 |
openSNP | rs2279709 |
23andMe | rs2279709 |
SNPshot | rs2279709 |
SNPdbe | rs2279709 |
MSV3d | rs2279709 |
GWAS Ctlg | rs2279709 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 28476685] Association study of the vesicular monoamine transporter 1 (VMAT1) gene with autism in an Iranian population.
[PMID 29536333] Association Study of VMAT1 Polymorphisms and Suicide Behavior.