rs11881940
A SNP in the HNRNPUL1 gene on chromosome 19. Its most notable genotype is A;A: normal form
- Gene
- HNRNPUL1
- Location
- Chr 1941,302,527 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 17%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A), (A;T), (T;T). 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.
- AverageA;A 74% A;T 23% T;T 4%
- European ancestry (Utah)A;A 77% A;T 23% T;T 0%
- Han Chinese (Beijing)A;A 60% A;T 26% T;T 14%
- Japanese (Tokyo)A;A 71% A;T 29% T;T 0%
- Yoruba (Nigeria)A;A 87% A;T 13% T;T 0%
Notes
From SNPedia
Notes
This SNP, located in an intron of a gene (HNRPUL1) on chromosome 19, may be associated with early onset myocardial infarction (MI). The risk allele for this SNP is the most common allele, rs11881940(A), with an odds ratio of 1.92 (1.28–2.86), and therefore it is also possible the view the rarer allele, rs11881940(T), as potentially playing a protective role against early onset MI.
Source and license
Adapted from rs11881940 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.