rs2287921
A SNP in the RASIP1 gene on chromosome 19. Its most notable genotype is C;T: common in complete genomics
- Gene
- RASIP1
- Location
- Chr 1948,725,015 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 26%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;T). 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.
- AverageC;T 24%
- European ancestry (Utah)C;T 45%
- Han Chinese (Beijing)C;T 7%
- Japanese (Tokyo)C;T 14%
- Yoruba (Nigeria)C;T 29%
Source and license
Adapted from rs2287921 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.