rs17174794
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs17174794(C;G) |
Make rs17174794(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 154089975 |
Gene | OPRM1 |
is a | snp |
is | mentioned by |
dbSNP | rs17174794 |
dbSNP (classic) | rs17174794 |
ClinGen | rs17174794 |
ebi | rs17174794 |
HLI | rs17174794 |
Exac | rs17174794 |
Gnomad | rs17174794 |
Varsome | rs17174794 |
LitVar | rs17174794 |
Map | rs17174794 |
PheGenI | rs17174794 |
Biobank | rs17174794 |
1000 genomes | rs17174794 |
hgdp | rs17174794 |
ensembl | rs17174794 |
geneview | rs17174794 |
scholar | rs17174794 |
rs17174794 | |
pharmgkb | rs17174794 |
gwascentral | rs17174794 |
openSNP | rs17174794 |
23andMe | rs17174794 |
SNPshot | rs17174794 |
SNPdbe | rs17174794 |
MSV3d | rs17174794 |
GWAS Ctlg | rs17174794 |
GMAF | 0.003214 |
Max Magnitude | 0 |
[PMID 23454283] Low frequency genetic variants in the μ-opioid receptor (OPRM1) affect risk for addiction to heroin and cocaine
ClinVar | |
---|---|
Risk | rs17174794(G;G) rs17174794(T;T) |
Alt | rs17174794(G;G) rs17174794(T;T) |
Reference | Rs17174794(C;C) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | OPRM1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000006.11:g.154411110C>G |
CLNSRC | |
CLNACC | RCV000238970.1, |