{{Rsnum
|rsid=1871922
|Gene=CNBP
|Chromosome=3
|position=129183756
|Orientation=plus
|GMAF=0.4555
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=CNBP
}}{{PMID Auto
|PMID=21224892
|Title=Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotype
|OA=1
}}{{PMID|12970845|OA=1
}} Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect.

{{PMID|19020295|OA=1
}} Premutation allele pool in myotonic dystrophy type 2.