{{Rsnum
|rsid=2273601
|Gene=ROS1
|Chromosome=6
|position=117409656
|Orientation=minus
|GMAF=0.2971
|Gene_s=ROS1
|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 | 50.4 | 43.4 | 6.2
| HCB | 58.1 | 32.4 | 9.6
| JPT | 46.9 | 45.1 | 8.0
| YRI | 19.0 | 42.2 | 38.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 58.1 | 32.4 | 9.6
| CHD | 48.6 | 45.9 | 5.5
| GIH | 20.8 | 52.5 | 26.7
| LWK | 34.9 | 45.0 | 20.2
| MEX | 73.7 | 22.8 | 3.5
| MKK | 39.7 | 46.8 | 13.5
| TSI | 62.7 | 30.4 | 6.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23459443
  |Trait=QT interval (interaction)
  |Title=Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.
  |RiskAllele=A
  |Pval=8E-6
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}