rs2118181
A SNP in the FBN1 gene on chromosome 15. Its most notable genotype is C;C: X1.8 higher risk of Thoracic aortic dissection.
- Gene
- FBN1
- Location
- Chr 1548,623,687 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CMost notableNot ratedX1.8 higher risk of Thoracic aortic dissection.
- C;TNot ratedX1.32 higher risk of thoracic aortic dissection
- T;TNot ratedNormal
On SNPedia: (C;C), (C;T), (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% C;T 40% T;T 46%
- European ancestry (Utah)C;C 2% C;T 17% T;T 81%
- Han Chinese (Beijing)C;C 10% C;T 36% T;T 54%
- Japanese (Tokyo)C;C 17% C;T 48% T;T 35%
- Yoruba (Nigeria)C;C 25% C;T 60% T;T 15%
- African ancestry (Southwest US)C;C 30% C;T 42% T;T 28%
- Chinese (Denver)C;C 6% C;T 37% T;T 58%
- Gujarati IndianC;C 2% C;T 30% T;T 68%
- Luhya (Kenya)C;C 32% C;T 49% T;T 19%
- Maasai (Kenya)C;C 14% C;T 56% T;T 30%
- TuscanC;C 2% C;T 29% T;T 69%
Related
Other FBN1 SNPs
- rs25404C;TFamilial thoracic aortic aneurysms and dissections (FTAAD)Very important
- rs140603C;GFamilial thoracic aortic aneurysms and dissections (FTAAD)Very important
- rs140630A;GFamilial thoracic aortic aneurysms and dissections (FTAAD)Very important
- rs111231312A;GFamilial thoracic aortic aneurysms and dissections (FTAAD)Very important
- rs111687884A;GFamilial thoracic aortic aneurysms and dissections (FTAAD)Very important
- rs112645512A;GFamilial thoracic aortic aneurysms and dissections (FTAAD)Very important
- rs112728248C;TFamilial thoracic aortic aneurysms and dissections (FTAAD)Very important
- rs112989722C;GFamilial thoracic aortic aneurysms and dissections (FTAAD)Very important
Notes
From SNPedia
Notes
Genetic variants in FBN-1 and risk for thoracic aortic aneurysm and dissection. Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1.
Source and license
Adapted from rs2118181 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.