rs2289030
A SNP in the KRT19P2 gene on chromosome 12. Its most notable genotype is G;G: common in complete genomics
- Gene
- KRT19P2
- Location
- Chr 1294,834,510 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
- Minor allele frequency
- 12%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2289030 on the minus strand: (C;C). 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.
- AverageG;G 72%
- European ancestry (Utah)G;G 82%
- Han Chinese (Beijing)G;G 59%
- Japanese (Tokyo)G;G 49%
- Yoruba (Nigeria)G;G 100%
Source and license
Adapted from rs2289030 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.