rs2442513
A SNP in the MCPH1 gene on chromosome 8. Its most notable genotype is T;T: common genotype
- Gene
- MCPH1
- Location
- Chr 86,439,029 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 7%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2442513 on the minus strand: (A;A), (C;C), (T;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 80% G;G 3% A;A 0%
- European ancestry (Utah)T;T 99% G;G 0% A;A 0%
- Han Chinese (Beijing)T;T 99% G;G 0% A;A 0%
- Japanese (Tokyo)T;T 99% G;G 0% A;A 0%
- Yoruba (Nigeria)T;T 56% G;G 6% A;A 0%
- African ancestry (Southwest US)T;T 58% G;G 5% A;A 0%
- Chinese (Denver)T;T 99% G;G 0% A;A 0%
- Gujarati IndianT;T 92% G;G 0% A;A 0%
- Luhya (Kenya)T;T 45% G;G 10% A;A 0%
- Mexican ancestry (Los Angeles)T;T 93% G;G 0% A;A 0%
- Maasai (Kenya)T;T 47% G;G 13% A;A 0%
- TuscanT;T 97% G;G 0% A;A 0%
Related
Other MCPH1 SNPs
- rs930557G;Gcommon in clinvarTypical
- rs1129703G;Gcommon in complete genomicsTypical
- rs1129706G;Gcommon in complete genomicsTypical
- rs2034143G;Gcommon in complete genomicsTypical
- rs2515569G;Gcommon in complete genomicsTypical
- rs2916733G;Gcommon in complete genomicsTypical
- rs12674488C;Ccommon in clinvarTypical
- rs17076812A;Acommon in complete genomicsTypical
Source and license
Adapted from rs2442513 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.