rs3948464
A SNP in the SP110 gene on chromosome 2. Its most notable genotype is G;G.
- Gene
- SP110
- Location
- Chr 2230,185,999 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 10%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs3948464 on the minus strand: (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 10 HapMap populations.
- AverageG;G 80% A;A 2%
- European ancestry (Utah)G;G 71% A;A 0%
- Han Chinese (Beijing)G;G 99% A;A 0%
- Japanese (Tokyo)G;G 100% A;A 0%
- Yoruba (Nigeria)G;G 76% A;A 3%
- African ancestry (Southwest US)G;G 79% A;A 2%
- Gujarati IndianG;G 91% A;A 1%
- Luhya (Kenya)G;G 57% A;A 2%
- Mexican ancestry (Los Angeles)G;G 90% A;A 2%
- Maasai (Kenya)G;G 57% A;A 8%
- TuscanG;G 81% A;A 0%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
associated with genetic susceptibility to tuberculosis in West Africa Variants in the SP110 gene are associated with genetic susceptibility to tuberculosis in West Africa. Polymorphisms in IL-1beta, vitamin D receptor Fok1, and Toll-like receptor 2 are associated with extrapulmonary tuberculosis. SP110 gene polymorphisms and tuberculosis susceptibility: A systematic review and meta-analysis based on 10 624 subjects.
Source and license
Adapted from rs3948464 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.