rs3810046
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3810046(A;A) |
Make rs3810046(A;C) |
Make rs3810046(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 6941663 |
Gene | LAMA1 |
is a | snp |
is | mentioned by |
dbSNP | rs3810046 |
dbSNP (classic) | rs3810046 |
ClinGen | rs3810046 |
ebi | rs3810046 |
HLI | rs3810046 |
Exac | rs3810046 |
Gnomad | rs3810046 |
Varsome | rs3810046 |
LitVar | rs3810046 |
Map | rs3810046 |
PheGenI | rs3810046 |
Biobank | rs3810046 |
1000 genomes | rs3810046 |
hgdp | rs3810046 |
ensembl | rs3810046 |
geneview | rs3810046 |
scholar | rs3810046 |
rs3810046 | |
pharmgkb | rs3810046 |
gwascentral | rs3810046 |
openSNP | rs3810046 |
23andMe | rs3810046 |
SNPshot | rs3810046 |
SNPdbe | rs3810046 |
MSV3d | rs3810046 |
GWAS Ctlg | rs3810046 |
GMAF | 0.3687 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22760553![]() |
Trait | Response to citalopram treatment |
Title | Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D. |
Risk Allele | T |
P-val | 5E-7 |
Odds Ratio | NR NR |