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rs17174794

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17174794(C;G)
Make rs17174794(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position154089975
GeneOPRM1
is asnp
is mentioned by
dbSNPrs17174794
dbSNP (classic)rs17174794
ClinGenrs17174794
ebirs17174794
HLIrs17174794
Exacrs17174794
Gnomadrs17174794
Varsomers17174794
LitVarrs17174794
Maprs17174794
PheGenIrs17174794
Biobankrs17174794
1000 genomesrs17174794
hgdprs17174794
ensemblrs17174794
geneviewrs17174794
scholarrs17174794
googlers17174794
pharmgkbrs17174794
gwascentralrs17174794
openSNPrs17174794
23andMers17174794
SNPshotrs17174794
SNPdbers17174794
MSV3drs17174794
GWAS Ctlgrs17174794
GMAF0.003214
Max Magnitude0

[PMID 23454283OA-icon.png] 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,