rs2107732
A SNP in the CCM2 gene on chromosome 7. Its most notable genotype is G;G: common on affy axiom data
- Gene
- CCM2
- Location
- Chr 745,038,379 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 5%
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 92%
- European ancestry (Utah)G;G 77%
- Han Chinese (Beijing)G;G 97%
- Japanese (Tokyo)G;G 97%
- Yoruba (Nigeria)G;G 99%
- African ancestry (Southwest US)G;G 96%
- Chinese (Denver)G;G 99%
- Gujarati IndianG;G 97%
- Luhya (Kenya)G;G 98%
- Mexican ancestry (Los Angeles)G;G 79%
- Maasai (Kenya)G;G 99%
- TuscanG;G 77%
Related
Other CCM2 SNPs
- rs137852841C;TCerebral Cavernous Malformation mutationVery important
- rs137852843G;TCerebral Cavernous Malformation mutationVery important
- rs797044623GC;TTCerebral Cavernous Malformation mutationVery important
- rs137852842A;GCerebral cavernous angioma associated mutation; variable penetranceVery important
- rs755800734C;TCerebral cavernous angioma associated mutation; variable penetranceVery important
- rs765548101C;GCerebral cavernous angioma associated mutation; variable penetranceVery important
- rs886041157C;TCerebral cavernous angioma associated mutation; variable penetranceVery important
- rs1057520070-;CCerebral cavernous angioma associated mutation; variable penetranceVery important
Source and license
Adapted from rs2107732 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.