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rs12466358

From SNPedia

Orientationplus
Stabilizedplus
Make rs12466358(G;G)
Make rs12466358(G;T)
Make rs12466358(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position232532815
GeneCHRND
is asnp
is mentioned by
dbSNPrs12466358
ebirs12466358
HLIrs12466358
Exacrs12466358
Varsomers12466358
Maprs12466358
PheGenIrs12466358
hapmaprs12466358
1000 genomesrs12466358
hgdprs12466358
ensemblrs12466358
gopubmedrs12466358
geneviewrs12466358
scholarrs12466358
googlers12466358
pharmgkbrs12466358
gwascentralrs12466358
openSNPrs12466358
23andMers12466358
23andMe allrs12466358
SNP Nexus

SNPshotrs12466358
SNPdbers12466358
MSV3drs12466358
GWAS Ctlgrs12466358
GMAF0.2704
Max Magnitude
? (G;G) (G;T) (T;T) 28
[PMID 20840187OA-icon.png] Peer smoking and the nicotinic receptor genes: an examination of genetic and environmental risks for nicotine dependence


[PMID 19259974OA-icon.png] Multiple distinct risk loci for nicotine dependence identified by dense coverage of the complete family of nicotinic receptor subunit (CHRN) genes.