rs3025035

A SNP in the VEGFA gene on chromosome 6. Its most notable genotype is C;C: common in complete genomics

Gene
VEGFA
Location
Chr 643,783,622 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
17%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in complete genomicsTypical · 0.066% of people

On SNPedia: (C;C). 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 66%
  • European ancestry (Utah)C;C 83%
  • Han Chinese (Beijing)C;C 67%
  • Japanese (Tokyo)C;C 57%
  • Yoruba (Nigeria)C;C 40%
  • African ancestry (Southwest US)C;C 35%
  • Chinese (Denver)C;C 72%
  • Gujarati IndianC;C 92%
  • Luhya (Kenya)C;C 55%
  • Mexican ancestry (Los Angeles)C;C 88%
  • Maasai (Kenya)C;C 57%
  • TuscanC;C 85%

Other VEGFA SNPs

All VEGFA SNPs

Notes

From SNPedia

Notes

Large-scale evaluation of candidate genes identifies associations between VEGF polymorphisms and bladder cancer risk. Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation. Polymorphisms in the VEGFA and VEGFR-2 genes and neovascular age-related macular degeneration. A two-step genetic study on quantitative precursors of coronary artery disease in a homogeneous Indian population: case-control association discovery and validation by transmission-disequilibrium test.

Source and license

Adapted from rs3025035 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.