rs1799972
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs1799972(C;T) |
Make rs1799972(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 154039561 |
Gene | OPRM1 |
is a | snp |
is | mentioned by |
dbSNP | rs1799972 |
dbSNP (classic) | rs1799972 |
ClinGen | rs1799972 |
ebi | rs1799972 |
HLI | rs1799972 |
Exac | rs1799972 |
Gnomad | rs1799972 |
Varsome | rs1799972 |
LitVar | rs1799972 |
Map | rs1799972 |
PheGenI | rs1799972 |
Biobank | rs1799972 |
1000 genomes | rs1799972 |
hgdp | rs1799972 |
ensembl | rs1799972 |
geneview | rs1799972 |
scholar | rs1799972 |
rs1799972 | |
pharmgkb | rs1799972 |
gwascentral | rs1799972 |
openSNP | rs1799972 |
23andMe | rs1799972 |
SNPshot | rs1799972 |
SNPdbe | rs1799972 |
MSV3d | rs1799972 |
GWAS Ctlg | rs1799972 |
GMAF | 0.06795 |
Max Magnitude | 0 |
[PMID 19103668] Expansion of the human mu-opioid receptor gene architecture: novel functional variants.
[PMID 20194481] Association of mu-opioid receptor variants and response to citalopram treatment in major depressive disorder.