rs11111419
A SNP in the PAH gene on chromosome 12. Its most notable genotype is A;A: common/normal
- Gene
- PAH
- Location
- Chr 12102,891,265 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
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 11 HapMap populations.
- AverageA;A 43%
- European ancestry (Utah)A;A 49%
- Han Chinese (Beijing)A;A 70%
- Japanese (Tokyo)A;A 66%
- Yoruba (Nigeria)A;A 19%
- African ancestry (Southwest US)A;A 25%
- Chinese (Denver)A;A 65%
- Gujarati IndianA;A 70%
- Luhya (Kenya)A;A 15%
- Mexican ancestry (Los Angeles)A;A 28%
- Maasai (Kenya)A;A 25%
- TuscanA;A 47%
Related
Other PAH SNPs
- rs5030841G;GPhenylketonuriaVery important
- rs5030843T;TPhenyketonuriaVery important
- rs5030846A;APhenyketonuriaVery important
- rs5030847A;APhenyketonuriaVery important
- rs5030849T;TPHENYLKETONURIA, MILDVery important
- rs5030850A;APhenyketonuriaVery important
- rs5030851A;APhenyketonuriaVery important
- rs5030852T;TPhenylketonuriaVery important
Source and license
Adapted from rs11111419 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.