{{Rsnum
|rsid=1978746
|Gene=ADAMTSL1
|Chromosome=9
|position=18761101
|Orientation=minus
|GMAF=0.141
|Gene_s=ADAMTSL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 4.4 | 29.2 | 66.4
| HCB | 1.5 | 33.6 | 65.0
| JPT | 0.0 | 18.6 | 81.4
| YRI | 0.0 | 2.0 | 98.0
| ASW | 0.0 | 5.4 | 94.6
| CHB | 1.5 | 33.6 | 65.0
| CHD | 0.9 | 20.4 | 78.7
| GIH | 5.9 | 27.7 | 66.3
| LWK | 0.0 | 0.0 | 0.0
| MEX | 3.5 | 43.9 | 52.6
| MKK | 0.6 | 3.8 | 95.5
| TSI | 5.9 | 33.3 | 60.8
| 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 v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}