rs3734355
A SNP in the LOC102724406 gene on chromosome 6. Its most notable genotype is G;G: common in clinvar
- Gene
- LOC102724406
- Location
- Chr 6100,420,845 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- FamilyTreeDNA
- Minor allele frequency
- 20%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs3734355 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 60%
- European ancestry (Utah)G;G 75%
- Han Chinese (Beijing)G;G 38%
- Japanese (Tokyo)G;G 25%
- Yoruba (Nigeria)G;G 100%
Source and license
Adapted from rs3734355 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.