rs1042034

A SNP in the APOB gene on chromosome 2. Its most notable genotype is C;C: common in clinvar

Gene
APOB
Location
Chr 221,002,409 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
34%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in clinvarTypical · 0.014% of people
  2. A;ANot ratedNo summary available.Typical · 0.00% of people

SNPedia records rs1042034 on the minus strand: (G;G), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 10 HapMap populations.

  • AverageC;C 14% A;A 0%
  • European ancestry (Utah)C;C 6% A;A 0%
  • Han Chinese (Beijing)C;C 44% A;A 0%
  • Japanese (Tokyo)C;C 46% A;A 0%
  • Yoruba (Nigeria)C;C 2% A;A 0%
  • African ancestry (Southwest US)C;C 0% A;A 0%
  • Gujarati IndianC;C 27% A;A 0%
  • Luhya (Kenya)C;C <1% A;A 0%
  • Mexican ancestry (Los Angeles)C;C 2% A;A 0%
  • Maasai (Kenya)C;C 3% A;A 0%
  • TuscanC;C 6% A;A 0%

Other APOB SNPs

All APOB SNPs

Source and license

Adapted from rs1042034 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.