{{Rsnum
|rsid=1926203
|Gene=ACTA2
|Chromosome=10
|position=90727334
|Orientation=minus
|GMAF=0.4601
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 10.6 | 44.2 | 45.1
| HCB | 78.8 | 19.7 | 1.5
| JPT | 84.1 | 14.2 | 1.8
| YRI | 21.8 | 49.0 | 29.3
| ASW | 15.8 | 43.9 | 40.4
| CHB | 78.8 | 19.7 | 1.5
| CHD | 70.6 | 26.6 | 2.8
| GIH | 51.5 | 45.5 | 3.0
| LWK | 22.7 | 51.8 | 25.5
| MEX | 31.0 | 46.6 | 22.4
| MKK | 26.3 | 48.7 | 25.0
| TSI | 14.7 | 45.1 | 40.2
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19654303
|Title=Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study
|OA=1
}}

{{PMID|21303977|OA=1
}} Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk.

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1926203
|overall_frequency_n=52
|overall_frequency_d=126
|overall_frequency=0.412698
|n_genomes=30
|n_genomes_annotated=0
|n_haplomes=41
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}