rs6974491
A SNP in the ELMO1 gene on chromosome 7. Its most notable genotype is A;A: Higher risk of coeliac and/or inflammatory bowel disease
- Gene
- ELMO1
- Location
- Chr 737,334,906 (GRCh38)
- Highest magnitude
- 1.5Minor
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 10%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBadHigher risk of coeliac and/or inflammatory bowel disease
- A;GBadHigher risk of coeliac and/or inflammatory bowel disease
- G;GGoodcommon on affy axiom data
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 10 HapMap populations.
- AverageA;A 1% A;G 16% G;G 82%
- European ancestry (Utah)A;A 3% A;G 25% G;G 72%
- Han Chinese (Beijing)A;A 0% A;G 2% G;G 99%
- Japanese (Tokyo)A;A 0% A;G 3% G;G 97%
- Yoruba (Nigeria)A;A 1% A;G 12% G;G 86%
- African ancestry (Southwest US)A;A 0% A;G 19% G;G 81%
- Gujarati IndianA;A 3% A;G 16% G;G 81%
- Luhya (Kenya)A;A 0% A;G 15% G;G 85%
- Mexican ancestry (Los Angeles)A;A 0% A;G 31% G;G 69%
- Maasai (Kenya)A;A 1% A;G 14% G;G 85%
- TuscanA;A 3% A;G 28% G;G 69%
Related
Source and license
Adapted from rs6974491 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.