rs2823256
A SNP in the LOC101927745 gene on chromosome 21. Its most notable genotype is A;A: normal risk of Crohn's disease in Koreans
- Gene
- LOC101927745
- Location
- Chr 2115,412,387 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableGoodnormal risk of Crohn's disease in Koreans
- A;GBad1.35x increased risk of Crohn's disease in Koreans
- G;GBad>1.32x increased risk of Crohn's disease in Koreans
On SNPedia: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageA;A 8% A;G 40% G;G 53%
- European ancestry (Utah)A;A 9% A;G 44% G;G 47%
- Han Chinese (Beijing)A;A 10% A;G 39% G;G 51%
- Japanese (Tokyo)A;A 7% A;G 43% G;G 50%
- Yoruba (Nigeria)A;A 3% A;G 25% G;G 73%
- African ancestry (Southwest US)A;A 2% A;G 35% G;G 63%
- Chinese (Denver)A;A 17% A;G 43% G;G 41%
- Gujarati IndianA;A 6% A;G 33% G;G 61%
- Luhya (Kenya)A;A 8% A;G 42% G;G 50%
- Mexican ancestry (Los Angeles)A;A 7% A;G 40% G;G 53%
- Maasai (Kenya)A;A 10% A;G 51% G;G 39%
- TuscanA;A 9% A;G 42% G;G 49%
Notes
From SNPedia
Notes
Implicated in a 2015 Korean cohort for Crohn's disease. PMID 25489960
Source and license
Adapted from rs2823256 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.