rs13224682
A SNP in the PRKAR2B gene on chromosome 7. Its most notable genotype is A;A: common on affy axiom data
- Gene
- PRKAR2B
- Location
- Chr 7107,122,773 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 3%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 8 HapMap populations.
- AverageA;A 93%
- European ancestry (Utah)A;A 85%
- Han Chinese (Beijing)A;A 99%
- Japanese (Tokyo)A;A 100%
- Yoruba (Nigeria)A;A 100%
- African ancestry (Southwest US)A;A 97%
- Gujarati IndianA;A 94%
- Mexican ancestry (Los Angeles)A;A 91%
- TuscanA;A 81%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
gwas, among 738 schizophrenics genotyped for 492K SNPs, this SNP attained a p-val of 6 x 10^-8 for triglycerides as a result of clozapine use
Source and license
Adapted from rs13224682 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.