rs1796390
A SNP in the PRICKLE1 gene on chromosome 12. Its most notable genotype is C;C: common/normal
- Gene
- PRICKLE1
- Location
- Chr 1242,484,802 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 24%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). 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.
- AverageC;C 58%
- European ancestry (Utah)C;C 58%
- Han Chinese (Beijing)C;C 45%
- Japanese (Tokyo)C;C 54%
- Yoruba (Nigeria)C;C 71%
- African ancestry (Southwest US)C;C 60%
- Chinese (Denver)C;C 60%
- Gujarati IndianC;C 54%
- Luhya (Kenya)C;C 53%
- Mexican ancestry (Los Angeles)C;C 76%
- Maasai (Kenya)C;C 52%
- TuscanC;C 55%
Related
Other PRICKLE1 SNPs
- rs113994140C;TCarrier of a progressive myoclonic epilepsy-1B mutationImportant
- rs281865564A;GCarrier of a progressive myoclonic epilepsy-1B mutationImportant
- rs557205452-;ATCCarrier of a progressive myoclonic epilepsy-1B mutationImportant
- rs1300341380C;TCarrier of a progressive myoclonic epilepsy-1B mutationImportant
Source and license
Adapted from rs1796390 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.