rs3732379
A SNP in the CX3CR1 gene on chromosome 3. Its most notable genotype is C;C: normal
- Gene
- CX3CR1
- Location
- Chr 339,265,765 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 17%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C), (C;T), (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.
- AverageC;C 77% C;T 20% T;T 2%
- European ancestry (Utah)C;C 55% C;T 38% T;T 7%
- Han Chinese (Beijing)C;C 98% C;T 2% T;T 0%
- Japanese (Tokyo)C;C 91% C;T 9% T;T 0%
- Yoruba (Nigeria)C;C 82% C;T 16% T;T 1%
- African ancestry (Southwest US)C;C 79% C;T 21% T;T 0%
- Chinese (Denver)C;C 97% C;T 3% T;T 0%
- Gujarati IndianC;C 73% C;T 25% T;T 2%
- Luhya (Kenya)C;C 85% C;T 16% T;T 0%
- Mexican ancestry (Los Angeles)C;C 59% C;T 35% T;T 7%
- Maasai (Kenya)C;C 76% C;T 23% T;T <1%
- TuscanC;C 55% C;T 38% T;T 8%
Related
Notes
From SNPedia
Notes
see also rs3732378
Source and license
Adapted from rs3732379 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.