{{Rsnum
|rsid=4254535
|Chromosome=2
|position=68971256
|Orientation=plus
|GMAF=0.2952
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 12.4 | 40.7 | 46.9
| HCB | 6.8 | 42.9 | 50.4
| JPT | 8.0 | 42.5 | 49.6
| YRI | 23.6 | 37.5 | 38.9
| ASW | 10.5 | 54.4 | 35.1
| CHB | 6.8 | 42.9 | 50.4
| CHD | 5.6 | 38.9 | 55.6
| GIH | 4.0 | 32.7 | 63.4
| LWK | 15.6 | 48.6 | 35.8
| MEX | 1.8 | 36.8 | 61.4
| MKK | 11.0 | 40.9 | 48.1
| TSI | 8.8 | 31.4 | 59.8
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19654303
|Trait=Lung cancer
|Title=Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study
|RiskAllele=
|Pval=0.000005
|OR=1.12
|ORtxt=[NR]
|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=rs4254535
|overall_frequency_n=44
|overall_frequency_d=128
|overall_frequency=0.34375
|n_genomes=33
|n_genomes_annotated=0
|n_haplomes=38
|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}}