rs699947
A SNP in the VEGFA gene on chromosome 6. Its most notable genotype is A;A: 1.36x increased risk for thyroid cancer in men
- Gene
- VEGFA
- Location
- Chr 643,768,652 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 34%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableNot rated1.36x increased risk for thyroid cancer in men
- A;CNot rated1.36x increased risk for thyroid cancer in men
- C;CNot ratednormal
On SNPedia: (A;A), (A;C), (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.
- AverageA;A 12% A;C 38% C;C 50%
- European ancestry (Utah)A;A 21% A;C 55% C;C 25%
- Han Chinese (Beijing)A;A 5% A;C 38% C;C 56%
- Japanese (Tokyo)A;A 17% A;C 39% C;C 44%
- Yoruba (Nigeria)A;A 2% A;C 24% C;C 74%
- African ancestry (Southwest US)A;A 0% A;C 33% C;C 67%
- Chinese (Denver)A;A 12% A;C 36% C;C 52%
- Gujarati IndianA;A 14% A;C 43% C;C 44%
- Luhya (Kenya)A;A 4% A;C 25% C;C 71%
- Mexican ancestry (Los Angeles)A;A 12% A;C 55% C;C 33%
- Maasai (Kenya)A;A 7% A;C 29% C;C 64%
- TuscanA;A 35% A;C 43% C;C 23%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs699947 (-2578C>A) is a SNP within close proximity of VEGFA (Vascular endothelial growth factor A). The A allele of rs699947 increased a risk for thyroid cancer (adjusted OR=1.36, 95% C.I=1.02~1.81, P=0.039) and regional lymph node metastasis only in men.
Source and license
Adapted from rs699947 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.