rs2067085
A SNP in the NOD2 gene on chromosome 16. Its most notable genotype is C;C: common in clinvar
- Gene
- NOD2
- Location
- Chr 1650,699,948 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 26%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageC;C 70%
- European ancestry (Utah)C;C 40%
- Han Chinese (Beijing)C;C 89%
- Japanese (Tokyo)C;C 96%
- Yoruba (Nigeria)C;C 56%
Related
Other NOD2 SNPs
- rs2066845C;C~35x higher risk for Crohn's diseaseVery important
- rs2066847C;C35x higher risk for Crohn's diseaseVery important
- rs2066844T;TSignificance unclear; possibly higher risk for Crohn's diseaseImportant
- rs2066843T;T4.09x higher risk for Crohn's diseaseWorth knowing
- rs17221417G;G1.9x higher risk for Crohn's diseaseWorth knowing
- rs5743289C;TPerhaps increased risk for certain autoinflammatory disordersMinor
- rs2066842C;Ccommon in clinvarTypical
- rs2076756A;AnormalTypical
Notes
From SNPedia
Notes
A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews. Evidence of allelic heterogeneity for associations between the NOD2/CARD15 gene and ulcerative colitis among North Indians. An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians. Association of NOD1 and NOD2 genes polymorphisms with Helicobacter pylori related gastric cancer in a Chinese population.
Source and license
Adapted from rs2067085 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.