Have questions? Visit https://www.reddit.com/r/SNPedia

rs1881492

From SNPedia

Orientationplus
Stabilizedplus
Make rs1881492(G;G)
Make rs1881492(G;T)
Make rs1881492(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position232542288
GeneCHRNG
is asnp
is mentioned by
dbSNPrs1881492
ebirs1881492
HLIrs1881492
Exacrs1881492
Varsomers1881492
Maprs1881492
PheGenIrs1881492
hapmaprs1881492
1000 genomesrs1881492
hgdprs1881492
ensemblrs1881492
gopubmedrs1881492
geneviewrs1881492
scholarrs1881492
googlers1881492
pharmgkbrs1881492
gwascentralrs1881492
openSNPrs1881492
23andMers1881492
23andMe allrs1881492
SNP Nexus

SNPshotrs1881492
SNPdbers1881492
MSV3drs1881492
GWAS Ctlgrs1881492
GMAF0.1887
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23396134OA-icon.png]
Trait Refractive error
Title Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
Risk Allele T
P-val 5E-11
Odds Ratio .14 [0.098-0.18] unit decrease


[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.