rs1367117
A SNP in the APOB gene on chromosome 2. Its most notable genotype is G;G: common in clinvar
- Gene
- APOB
- Location
- Chr 221,041,028 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 21%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (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.
- AverageG;G 72%
- European ancestry (Utah)G;G 45%
- Han Chinese (Beijing)G;G 83%
- Japanese (Tokyo)G;G 84%
- Yoruba (Nigeria)G;G 86%
- African ancestry (Southwest US)G;G 68%
- Chinese (Denver)G;G 76%
- Gujarati IndianG;G 78%
- Luhya (Kenya)G;G 86%
- Mexican ancestry (Los Angeles)G;G 53%
- Maasai (Kenya)G;G 82%
- TuscanG;G 49%
Related
Other APOB SNPs
- i4000339A;AFamilial Hypercholesterolemia Type BVery important
- rs5742904A;CFamilial HypercholesterolemiaVery important
- rs144467873A;Afamilial hypercholesterolemiaVery important
- rs730880052G;TFamilial HypercholesterolemiaVery important
- rs886039829-;THypercholesterolemia, Type B; heterozygoteImportant
- rs12713559A;Gcarrier of possible familial hypercholesterolemia mutationImportant
- rs121918383A;GCarrier of a hypobetalipoproteinemia mutationImportant
- rs121918384-;GTCarrier of a hypobetalipoproteinemia mutationImportant
Notes
From SNPedia
Notes
rs1367117 (C711T/711C>T) is a SNP within APOB (Apolipoprotein B). associated with apoB levels
Source and license
Adapted from rs1367117 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.