{{Rsnum
|rsid=10838687
|Gene=MADD
|Chromosome=11
|position=47291341
|Orientation=plus
|GMAF=0.382
|Gene_s=MADD
|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 | 2.7 | 32.7 | 64.6
| HCB | 37.2 | 44.5 | 18.2
| JPT | 44.6 | 42.9 | 12.5
| YRI | 23.8 | 53.1 | 23.1
| ASW | 10.5 | 52.6 | 36.8
| CHB | 37.2 | 44.5 | 18.2
| CHD | 48.1 | 35.2 | 16.7
| GIH | 9.9 | 38.6 | 51.5
| LWK | 17.3 | 39.1 | 43.6
| MEX | 10.3 | 39.7 | 50.0
| MKK | 16.7 | 42.3 | 41.0
| TSI | 1.0 | 25.5 | 73.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21873549
|Trait=None
|Title=Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.
|RiskAllele=T
|Pval=7E-12
|OR=None
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=24951664
|Title=Association of Levels of Fasting Glucose and Insulin With Rare Variants at the Chromosome 11p11.2-MADD Locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study
}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}