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rs886716

From SNPedia

Orientationplus
Stabilizedplus
Make rs886716(A;A)
Make rs886716(A;G)
Make rs886716(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position26517999
is asnp
is mentioned by
dbSNPrs886716
ebirs886716
HLIrs886716
Exacrs886716
Varsomers886716
Maprs886716
PheGenIrs886716
hapmaprs886716
1000 genomesrs886716
hgdprs886716
ensemblrs886716
gopubmedrs886716
geneviewrs886716
scholarrs886716
googlers886716
pharmgkbrs886716
gwascentralrs886716
openSNPrs886716
23andMers886716
23andMe allrs886716
SNP Nexus

SNPshotrs886716
SNPdbers886716
MSV3drs886716
GWAS Ctlgrs886716
GMAF0.3118
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19247474OA-icon.png]
Trait Smoking behaviors
Title Genome-wide and candidate gene association study of cigarette smoking behaviors
Risk Allele
P-val 0.000008
Odds Ratio 1.52 [NR]



GET Evidence
rs886716
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.40625
summary