rs10227893
A SNP in the FOXP2 gene on chromosome 7. Its most notable genotype is T;T: common in complete genomics
- Gene
- FOXP2
- Location
- Chr 7114,630,022 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 12%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (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.
- AverageT;T 72%
- European ancestry (Utah)T;T 89%
- Han Chinese (Beijing)T;T 100%
- Japanese (Tokyo)T;T 100%
- Yoruba (Nigeria)T;T 52%
- African ancestry (Southwest US)T;T 41%
- Gujarati IndianT;T 85%
- Luhya (Kenya)T;T 46%
- Mexican ancestry (Los Angeles)T;T 84%
- Maasai (Kenya)T;T 36%
- TuscanT;T 87%
Related
Other FOXP2 SNPs
- rs121908377A;Gspeech and other processing issuesImportant
- rs121908378C;Tspeech and other processing issuesImportant
- rs786200976-;Aspeech and other processing issues possibleImportant
- rs879253770-;ACAACAGCAGCAspeech and other processing issues possibleImportant
- rs879253771-;CAspeech and other processing issues possibleImportant
- rs879253772C;Tspeech and other processing issues possibleImportant
- rs1064793842-;Gspeech and other processing issues possibleImportant
Notes
From SNPedia
Notes
variations in rs17137124 and rs10227893 may impair speech
Source and license
Adapted from rs10227893 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.