rs2270637
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2270637(C;C) |
Make rs2270637(C;G) |
Make rs2270637(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 8 |
Position | 20179316 |
Gene | SLC18A1 |
is a | snp |
is | mentioned by |
dbSNP | rs2270637 |
dbSNP (classic) | rs2270637 |
ClinGen | rs2270637 |
ebi | rs2270637 |
HLI | rs2270637 |
Exac | rs2270637 |
Gnomad | rs2270637 |
Varsome | rs2270637 |
LitVar | rs2270637 |
Map | rs2270637 |
PheGenI | rs2270637 |
Biobank | rs2270637 |
1000 genomes | rs2270637 |
hgdp | rs2270637 |
ensembl | rs2270637 |
geneview | rs2270637 |
scholar | rs2270637 |
rs2270637 | |
pharmgkb | rs2270637 |
gwascentral | rs2270637 |
openSNP | rs2270637 |
23andMe | rs2270637 |
SNPshot | rs2270637 |
SNPdbe | rs2270637 |
MSV3d | rs2270637 |
GWAS Ctlg | rs2270637 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
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[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.