rs2857708
A SNP in the LOC100287329 gene on chromosome 6. Its most notable genotype is C;C: common in complete genomics
- Gene
- LOC100287329
- Location
- Chr 631,565,829 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 10%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2857708 on the minus strand: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageC;C 84%
- European ancestry (Utah)C;C 74%
- Han Chinese (Beijing)C;C 79%
- Japanese (Tokyo)C;C 81%
- Yoruba (Nigeria)C;C 95%
- African ancestry (Southwest US)C;C 95%
- Chinese (Denver)C;C 74%
- Gujarati IndianC;C 85%
- Luhya (Kenya)C;C 95%
- Mexican ancestry (Los Angeles)C;C 77%
- Maasai (Kenya)C;C 97%
- TuscanC;C 78%
Related
Other LOC100287329 SNPs
- rs1041981A;AHigher myocardial infarction riskWorth knowing
- rs1799724C;Tif ApoE4(-), 1.6x risk of AD; if (+), 6.6x riskWorth knowing
- rs1800630A;A1.8x increased lupus riskTypical
- rs2230365C;Ccommon in complete genomicsTypical
- rs3130062T;Tcommon on affy axiom dataTypical
- rs7762619T;Tcommon in complete genomicsTypical
Source and license
Adapted from rs2857708 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.