rs10965235
A SNP in the CDKN2B-AS1 gene on chromosome 9. Its most notable genotype is C;C: common in complete genomics
- Gene
- CDKN2B-AS1
- Location
- Chr 922,115,106 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 18%
Genotypes
As shown in 23andMe and AncestryDNA files.
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 61%
- European ancestry (Utah)C;C 100%
- Han Chinese (Beijing)C;C 71%
- Japanese (Tokyo)C;C 65%
- Yoruba (Nigeria)C;C 17%
- African ancestry (Southwest US)C;C 32%
- Chinese (Denver)C;C 64%
- Gujarati IndianC;C 91%
- Luhya (Kenya)C;C 18%
- Mexican ancestry (Los Angeles)C;C 95%
- Maasai (Kenya)C;C 19%
- TuscanC;C 98%
Related
Other CDKN2B-AS1 SNPs
- rs10757272T;T1.54x increased risk for Coronary artery diseaseWorth knowing
- rs4977574G;GMost studies find a somewhat elevated (~1.5x) risk for myocardial infarctionMinor
- rs17756311A;APossible higher risk of childhood acute lymphoblastic leukemiaMinor
- rs1011970G;Gcommon in complete genomicsTypical
- rs10116277G;TNo summary available.Typical
- rs10757274A;AnormalTypical
Source and license
Adapted from rs10965235 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.