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rs1889899

From SNPedia

Orientationplus
Stabilizedplus
Make rs1889899(A;A)
Make rs1889899(A;G)
Make rs1889899(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position26789942
is asnp
is mentioned by
dbSNPrs1889899
ebirs1889899
HLIrs1889899
Exacrs1889899
Varsomers1889899
Maprs1889899
PheGenIrs1889899
hapmaprs1889899
1000 genomesrs1889899
hgdprs1889899
ensemblrs1889899
gopubmedrs1889899
geneviewrs1889899
scholarrs1889899
googlers1889899
pharmgkbrs1889899
gwascentralrs1889899
openSNPrs1889899
23andMers1889899
23andMe allrs1889899
SNP Nexus

SNPshotrs1889899
SNPdbers1889899
MSV3drs1889899
GWAS Ctlgrs1889899
GMAF0.2727
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 0.000006
Odds Ratio 1.26 [NR]



GET Evidence
rs1889899
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.289062
summary