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rs10989661

From SNPedia

Orientationplus
Stabilizedplus
Make rs10989661(A;A)
Make rs10989661(A;G)
Make rs10989661(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position101860586
is asnp
is mentioned by
dbSNPrs10989661
ebirs10989661
HLIrs10989661
Exacrs10989661
Varsomers10989661
Maprs10989661
PheGenIrs10989661
hapmaprs10989661
1000 genomesrs10989661
hgdprs10989661
ensemblrs10989661
gopubmedrs10989661
geneviewrs10989661
scholarrs10989661
googlers10989661
pharmgkbrs10989661
gwascentralrs10989661
openSNPrs10989661
23andMers10989661
23andMe allrs10989661
SNP Nexus

SNPshotrs10989661
SNPdbers10989661
MSV3drs10989661
GWAS Ctlgrs10989661
GMAF0.191
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 1.68 [NR]



GET Evidence
rs10989661
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.203125
summary