rs529038

A SNP in the ROS1 gene on chromosome 6. Its most notable genotype is T;T.

Gene
ROS1
Location
Chr 6117,301,070 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
16%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableNot ratedNo summary available.Typical · 0.03% of people
  2. A;GNot ratedNo summary available.Typical · 0.00% of people

SNPedia records rs529038 on the minus strand: (A;A), (C;T). 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 3% A;G 0%
  • European ancestry (Utah)T;T 8% A;G 0%
  • Han Chinese (Beijing)T;T 2% A;G 0%
  • Japanese (Tokyo)T;T 2% A;G 0%
  • Yoruba (Nigeria)T;T 0% A;G 0%
  • African ancestry (Southwest US)T;T 0% A;G 0%
  • Chinese (Denver)T;T 4% A;G 0%
  • Gujarati IndianT;T 2% A;G 0%
  • Luhya (Kenya)T;T 0% A;G 0%
  • Mexican ancestry (Los Angeles)T;T 3% A;G 0%
  • Maasai (Kenya)T;T 2% A;G 0%
  • TuscanT;T 6% A;G 0%

Other ROS1 SNPs

All ROS1 SNPs

Notes

From SNPedia

Notes

rs529038, also known as Asp2213Asn, is not associated with coronary artery disease in a Greek case-control study of ~300 patients. Identification of four gene variants associated with myocardial infarction. Association of genetic variants with atherothrombotic cerebral infarction in Japanese individuals with metabolic syndrome. Replication study of 10 genetic polymorphisms associated with coronary heart disease in a specific high-risk population with familial hypercholesterolemia.

Source and license

Adapted from rs529038 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.