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rs114216682

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs114216682(C;C)
Make rs114216682(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position53405413
is asnp
is mentioned by
dbSNPrs114216682
ebirs114216682
HLIrs114216682
Exacrs114216682
Varsomers114216682
Maprs114216682
PheGenIrs114216682
hapmaprs114216682
1000 genomesrs114216682
hgdprs114216682
ensemblrs114216682
gopubmedrs114216682
geneviewrs114216682
scholarrs114216682
googlers114216682
pharmgkbrs114216682
gwascentralrs114216682
openSNPrs114216682
23andMers114216682
23andMe allrs114216682
SNP Nexus

SNPshotrs114216682
SNPdbers114216682
MSV3drs114216682
GWAS Ctlgrs114216682
GMAF0.00551
Max Magnitude0
GWAS snp
PMID [PMID 21685187OA-icon.png]
Trait
Title Genome-wide association study of smoking behaviours in patients with COPD.
Risk Allele G
P-val 7E-8
Odds Ratio 4.4900 [NR]