{{Rsnum
|rsid=1889899
|Chromosome=9
|position=26789942
|Orientation=plus
|GMAF=0.2727
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 33.6 | 54.9 | 11.5
| HCB | 77.9 | 20.6 | 1.5
| JPT | 64.6 | 33.6 | 1.8
| YRI | 59.2 | 38.1 | 2.7
| ASW | 61.4 | 31.6 | 7.0
| CHB | 77.9 | 20.6 | 1.5
| CHD | 71.6 | 25.7 | 2.8
| GIH | 56.4 | 38.6 | 5.0
| LWK | 66.4 | 25.5 | 8.2
| MEX | 56.9 | 32.8 | 10.3
| MKK | 55.8 | 36.5 | 7.7
| TSI | 31.4 | 52.9 | 15.7
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19247474
|Trait=Smoking behaviors
|Title=Genome-wide and candidate gene association study of cigarette smoking behaviors
|RiskAllele=
|Pval=0.000006
|OR=1.26
|ORtxt=[NR]
|OA=1
}}

{{PharmGKB
|RSID=rs1889899
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:19247474; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Genome-wide and candidate gene association study of cigarette Smoking behaviors. (Initial Sample Size: 4,611 individuals (2,617 smokers); Replication Sample Size: NR); (Region: 9p21.2; Reported Gene(s): Intergenic); (p-value= 0.000006).This variant is associated with Smoking behaviors.
|Drugs=
|Drug Classes=
|Diseases=Tobacco Use Disorder
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164739948
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1889899
|overall_frequency_n=37
|overall_frequency_d=128
|overall_frequency=0.289062
|n_genomes=24
|n_genomes_annotated=0
|n_haplomes=26
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}