rs1046089
A SNP in the PRRC2A gene on chromosome 6. Its most notable genotype is A;A: normal
- Gene
- PRRC2A
- Location
- Chr 631,635,190 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 39%
Genotypes
As shown in 23andMe and AncestryDNA files.
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 18% A;G 45% G;G 38%
- European ancestry (Utah)A;A 9% A;G 43% G;G 49%
- Han Chinese (Beijing)A;A 15% A;G 53% G;G 32%
- Japanese (Tokyo)A;A 13% A;G 43% G;G 44%
- Yoruba (Nigeria)A;A 40% A;G 40% G;G 20%
- African ancestry (Southwest US)A;A 32% A;G 47% G;G 21%
- Chinese (Denver)A;A 17% A;G 45% G;G 38%
- Gujarati IndianA;A 6% A;G 38% G;G 56%
- Luhya (Kenya)A;A 30% A;G 44% G;G 26%
- Mexican ancestry (Los Angeles)A;A 9% A;G 42% G;G 49%
- Maasai (Kenya)A;A 21% A;G 46% G;G 33%
- TuscanA;A 7% A;G 49% G;G 44%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs1046089 is a SNP in the HLA-B associated transcript 2 BAT2 gene. A study of 2,162 case-controls found an association between rs1046089 and severe malaria.
Source and license
Adapted from rs1046089 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.