{{Rsnum
|rsid=1530057
|Gene=RBMS3
|Chromosome=3
|position=29533972
|Orientation=minus
|GMAF=0.04591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=RBMS3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.0 | 8.8 | 91.2
| HCB | 1.5 | 18.2 | 80.3
| JPT | 0.0 | 14.2 | 85.8
| YRI | 0.0 | 0.7 | 99.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 1.5 | 18.2 | 80.3
| CHD | 0.0 | 17.4 | 82.6
| GIH | 1.0 | 16.8 | 82.2
| LWK | 0.0 | 1.8 | 98.2
| MEX | 3.4 | 19.0 | 77.6
| MKK | 0.0 | 0.6 | 99.4
| TSI | 0.0 | 4.9 | 95.1
| 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=0.000003
|OR=1.26
|ORtxt=[NR]
|OA=1
}}

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

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1530057
|overall_frequency_n=3
|overall_frequency_d=128
|overall_frequency=0.0234375
|n_genomes=3
|n_genomes_annotated=0
|n_haplomes=4
|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}}