rs1042031
A SNP in the APOB gene on chromosome 2. Its most notable genotype is T;T.
- Gene
- APOB
- Location
- Chr 221,002,881 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 15%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TMost notableNot ratedNo summary available.
- G;GNot ratedNo summary available.
- C;CGoodcommon in clinvar
SNPedia records rs1042031 on the minus strand: (A;A), (C;C), (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.
- AverageT;T 2% G;G 0% C;C 77%
- European ancestry (Utah)T;T 6% G;G 0% C;C 66%
- Han Chinese (Beijing)T;T 0% G;G 0% C;C 94%
- Japanese (Tokyo)T;T 0% G;G 0% C;C 92%
- Yoruba (Nigeria)T;T 4% G;G 0% C;C 71%
- African ancestry (Southwest US)T;T 4% G;G 0% C;C 70%
- Chinese (Denver)T;T 0% G;G 0% C;C 94%
- Gujarati IndianT;T 4% G;G 0% C;C 85%
- Luhya (Kenya)T;T 5% G;G 0% C;C 62%
- Mexican ancestry (Los Angeles)T;T 2% G;G 0% C;C 66%
- Maasai (Kenya)T;T 1% G;G 0% C;C 84%
- TuscanT;T 1% G;G 0% C;C 67%
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
Source and license
Adapted from rs1042031 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.