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rs912969

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs912969(C;T)
Make rs912969(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position103214754
is asnp
is mentioned by
dbSNPrs912969
ebirs912969
HLIrs912969
Exacrs912969
Varsomers912969
Maprs912969
PheGenIrs912969
hapmaprs912969
1000 genomesrs912969
hgdprs912969
ensemblrs912969
gopubmedrs912969
geneviewrs912969
scholarrs912969
googlers912969
pharmgkbrs912969
gwascentralrs912969
openSNPrs912969
23andMers912969
23andMe allrs912969
SNP Nexus

SNPshotrs912969
SNPdbers912969
MSV3drs912969
GWAS Ctlgrs912969
GMAF0.2208
Max Magnitude0
? (C;C) (C;T) (T;T) 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 0.14 [NR] fewer years



GET Evidence
rs912969
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.25
summary