{{Rsnum
|rsid=7111341
|Chromosome=11
|position=2191936
|Orientation=plus
|GMAF=0.253
|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 | 46.9 | 43.4 | 9.7
| HCB | 83.8 | 14.7 | 1.5
| JPT | 85.8 | 14.2 | 0.0
| YRI | 30.8 | 43.8 | 25.3
| ASW | 36.8 | 56.1 | 7.0
| CHB | 83.8 | 14.7 | 1.5
| CHD | 83.5 | 14.7 | 1.8
| GIH | 70.3 | 27.7 | 2.0
| LWK | 20.2 | 56.0 | 23.9
| MEX | 77.6 | 17.2 | 5.2
| MKK | 46.8 | 44.9 | 8.3
| TSI | 53.9 | 40.2 | 5.9
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19430480
|Trait=Type 1 diabetes
|Title=Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
|RiskAllele=
|Pval=4E-48
|OR=NR
|ORtxt=NR
|OA=1
}}

{{omim
|id=125852
|rsnum=7111341
}}

{{omim
|id=222100
|rsnum=7111341
}}

{{PMID Auto
|PMID=19966805
|Title=The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7111341
|overall_frequency_n=36
|overall_frequency_d=128
|overall_frequency=0.28125
|n_genomes=29
|n_genomes_annotated=0
|n_haplomes=37
|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}}