rs7190458

A SNP in the BCAR1 gene on chromosome 16. Its most notable genotype is A;A: Higher pancreatic cancer risk

Gene
BCAR1
Location
Chr 1675,229,763 (GRCh38)
Highest magnitude
2.1Worth knowing
Tested on
23andMe, AncestryDNA, FamilyTreeDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableBadHigher pancreatic cancer riskWorth knowing · 2.12% of people
  2. A;GBadSlightly higher pancreatic cancer riskWorth knowing · 2.019% of people
  3. G;GGoodcommon genotypeTypical · 0.079% of people

On SNPedia: (A;A), (A;G), (G;G). 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.

  • AverageA;A 2% A;G 19% G;G 79%
  • European ancestry (Utah)A;A <1% A;G 10% G;G 89%
  • Han Chinese (Beijing)A;A 0% A;G 4% G;G 96%
  • Japanese (Tokyo)A;A 0% A;G 3% G;G 97%
  • Yoruba (Nigeria)A;A 10% A;G 43% G;G 47%
  • African ancestry (Southwest US)A;A 2% A;G 40% G;G 58%
  • Chinese (Denver)A;A 0% A;G 6% G;G 95%
  • Luhya (Kenya)A;A 7% A;G 32% G;G 61%
  • Mexican ancestry (Los Angeles)A;A 0% A;G 14% G;G 86%
  • Maasai (Kenya)A;A 5% A;G 31% G;G 64%
  • TuscanA;A 0% A;G 5% G;G 95%

Conditions, medicines and genes

Notes

From SNPedia

Notes

A 2014 study "Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer" of 7,683 European cases and 14,397 controls found the minor allele rs7190458(A) in BCAR1 (breast cancer anti-estrogen resistance 1) conferring risk of statistically genome-wide significance (per-allele odds ratio (OR) = 1.46, 95% confidence interval (CI) 1.30-1.65, P = 1.1E-10) for Pancreatic cancer.

Source and license

Adapted from rs7190458 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.