{{Rsnum
|rsid=1017
|Gene=ISL1
|Chromosome=5
|position=51394261
|Orientation=plus
|GMAF=0.3669
|Gene_s=ISL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{PMID Auto
|PMID=22480195
|Title=ISL1 Common Variant rs1017 Is Not Associated with Susceptibility to Congenital Heart Disease in a Chinese Population
|OA=1
}}{{PMID Auto
|PMID=20520780
|Title=Common variation in ISL1 confers genetic susceptibility for human congenital heart disease.
|OA=1
}}{{PMID Auto
|PMID=23229290
|Title=Lack of association of the 3'-UTR polymorphism (rs1017) in the ISL1 gene and risk of congenital heart disease in the white population.
}}

{{PMID Auto
|PMID=23572340
|Title=Association between ISL1 variants and susceptibility to ventricular septal defect in a Chinese cohort.
}}