{{Rsnum
|rsid=10936599
|Gene=MYNN
|Chromosome=3
|position=169774313
|Orientation=plus
|GMAF=0.3035
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MYNN
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 53.1 | 39.8 | 7.1
| HCB | 14.6 | 57.7 | 27.7
| JPT | 8.0 | 47.8 | 44.2
| YRI | 98.6 | 1.4 | 0.0
| ASW | 84.2 | 14.0 | 1.8
| CHB | 14.6 | 57.7 | 27.7
| CHD | 22.0 | 46.8 | 31.2
| GIH | 62.4 | 32.7 | 5.0
| LWK | 83.6 | 15.5 | 0.9
| MEX | 37.9 | 53.4 | 8.6
| MKK | 82.1 | 16.7 | 1.3
| TSI | 64.7 | 32.4 | 2.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20190752
|Trait=Celiac disease
|Title=Multiple common variants for celiac disease influencing immune gene expression
|RiskAllele=A
|Pval=5E-7
|OR=1.12
|ORtxt=[1.07-1.16]
|OA=1
}}

{{PMID Auto GWAS
|PMID=20972440
|Trait=None
|Title=Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
|RiskAllele=C
|Pval=3E-8
|OR=1.0400
|ORtxt=[1.04-1.10]
}}

{{PMID Auto
|PMID=21708826
|Title=TERC polymorphisms are associated both with susceptibility to colorectal cancer and with longer telomeres
|OA=1
}}

{{PMID Auto GWAS
|PMID=21833088
|Trait=None
|Title=Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
|RiskAllele=G
|Pval=7E-7
|OR=1.1000
|ORtxt=[1.08-1.11]
|OA=1
}}

{{PMID Auto
|PMID=22045029
|Title=Relationship between 16 susceptibility loci and colorectal cancer phenotype in 3146 patients.
}}

{{PMID Auto GWAS
  |PMID=23535734
  |Trait=Telomere length
  |Title=Identification of seven loci affecting mean telomere length and their association with disease.
  |RiskAllele=T
  |Pval=3E-31
  |OR=.10
  |ORtxt=[0.081-0.113] unit decrease
  |OA=1
}}

{{PMID Auto
|PMID=24449210
|Title=Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
}}

{{PMID Auto
|PMID=24292274
|Title=A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia
}}

{{PMID Auto
|PMID=22999960
|Title=Much of the genetic risk of colorectal cancer is likely to be mediated through susceptibility to adenomas.
|OA=1
}}

{{PMID Auto GWAS
  |PMID=24163127
  |Trait=Bladder cancer
  |Title=Genome-wide association study identifies multiple loci associated with bladder cancer risk.
  |RiskAllele=C
  |Pval=5E-9
  |OR=1.18
  |ORtxt=[1.11-1.23]
  }}

{{PMID Auto
|PMID=24875374
|Title=Variation in the Association Between Colorectal Cancer Susceptibility Loci and Colorectal Polyps by Polyp Type
}}

{{PMID Auto
|PMID=24904205
|Title=Association between previously identified loci affecting telomere length and coronary heart disease (CHD) in Han Chinese population
}}

{{PMID Auto
|PMID=24978480
|Title=A Colorectal Cancer Susceptibility New Variant at 4q26 in the Spanish Population Identified by Genome-Wide Association Analysis
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}