rs2075822
A SNP in the NOD1 gene on chromosome 7. Its most notable genotype is A;A: common in complete genomics
- Gene
- NOD1
- Location
- Chr 730,451,144 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 20%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2075822 on the minus strand: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Notes
From SNPedia
Notes
Association of NOD1 polymorphisms with atopic eczema and related phenotypes. The role of microorganisms in atopic dermatitis. A functional variant in the CARD4 gene and risk of premature coronary heart disease. Toll-like receptor (TLR) and nucleosome-binding oligomerization domain (NOD) gene polymorphisms and endometrial cancer risk. Role of NOD1/CARD4 and NOD2/CARD15 gene polymorphisms in cancer etiology. Association of NOD1 and NOD2 genes polymorphisms with Helicobacter pylori related gastric cancer in a Chinese population.
Source and license
Adapted from rs2075822 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.