rs10244329
A SNP in the LEP gene on chromosome 7. Its most notable genotype is A;T: common in complete genomics
- Gene
- LEP
- Location
- Chr 7128,248,636 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 45%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;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.
- AverageA;T 47%
- European ancestry (Utah)A;T 50%
- Han Chinese (Beijing)A;T 35%
- Japanese (Tokyo)A;T 40%
- Yoruba (Nigeria)A;T 54%
- African ancestry (Southwest US)A;T 53%
- Chinese (Denver)A;T 44%
- Gujarati IndianA;T 42%
- Luhya (Kenya)A;T 52%
- Mexican ancestry (Los Angeles)A;T 45%
- Maasai (Kenya)A;T 51%
- TuscanA;T 52%
Related
Source and license
Adapted from rs10244329 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.