rs12730292
A SNP on chromosome 1. Its most notable genotype is C;G: common in complete genomics
- Gene
- None listed
- Location
- Chr 178,789,077 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
- Minor allele frequency
- 22%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;G). 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;G 20%
- European ancestry (Utah)C;G 45%
- Han Chinese (Beijing)C;G 11%
- Japanese (Tokyo)C;G 2%
- Yoruba (Nigeria)C;G 21%
Source and license
Adapted from rs12730292 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.