{{Rsnum
|rsid=1077861
|Gene=NOD2
|Chromosome=16
|position=50725636
|Orientation=minus
|GMAF=0.3893
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=NOD2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 50.4 | 42.5 | 7.1
| HCB | 3.6 | 32.8 | 63.5
| JPT | 3.5 | 28.3 | 68.1
| YRI | 2.0 | 34.7 | 63.3
| ASW | 12.3 | 31.6 | 56.1
| CHB | 3.6 | 32.8 | 63.5
| CHD | 2.8 | 22.9 | 74.3
| GIH | 11.9 | 33.7 | 54.5
| LWK | 4.6 | 33.0 | 62.4
| MEX | 20.7 | 39.7 | 39.7
| MKK | 23.7 | 54.5 | 21.8
| TSI | 48.5 | 41.6 | 9.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=21943069
|Title=A NOD2 gene polymorphism is associated with the prevalence and severity of chronic obstructive pulmonary disease in a Japanese population
}}

{{PMID|12019468|OA=1
}} CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure.

{{PMID|12577202|OA=1
}} A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews.

{{PMID|16008671}} Association of CARD15 polymorphisms with atopy-related traits in a population-based cohort of Caucasian adults.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}