rs1011970
A SNP in the CDKN2B-AS1 gene on chromosome 9. Its most notable genotype is G;G: common in complete genomics
- Gene
- CDKN2B-AS1
- Location
- Chr 922,062,135 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 22%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G). 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.
- AverageG;G 62%
- European ancestry (Utah)G;G 71%
- Han Chinese (Beijing)G;G 83%
- Japanese (Tokyo)G;G 93%
- Yoruba (Nigeria)G;G 38%
- African ancestry (Southwest US)G;G 54%
- Chinese (Denver)G;G 86%
- Gujarati IndianG;G 66%
- Luhya (Kenya)G;G 29%
- Mexican ancestry (Los Angeles)G;G 35%
- Maasai (Kenya)G;G 56%
- TuscanG;G 69%
Related
Conditions, medicines and genes
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
- rs10116277G;TNo summary available.Typical
- rs10757274A;AnormalTypical
- rs10965235C;Ccommon in complete genomicsTypical
Notes
From SNPedia
Notes
in Chinese women no significant breast cancer association at rs1011970, rs10757278 or rs2380205
Source and license
Adapted from rs1011970 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.