rs3769048
A SNP in the RAMP1 gene on chromosome 2. Its most notable genotype is G;G: common in complete genomics
- Gene
- RAMP1
- Location
- Chr 2237,861,218 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
- Minor allele frequency
- 8%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs3769048 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 8 HapMap populations.
- AverageG;G 78%
- European ancestry (Utah)G;G 99%
- Han Chinese (Beijing)G;G 63%
- Japanese (Tokyo)G;G 43%
- Yoruba (Nigeria)G;G 92%
- Chinese (Denver)G;G 64%
- Gujarati IndianG;G 82%
- Mexican ancestry (Los Angeles)G;G 86%
- Maasai (Kenya)G;G 96%
Source and license
Adapted from rs3769048 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.