rs5968255
A SNP on chromosome X. Its most notable genotype is C;C: slower AIDS progression (8 years)
- Gene
- None listed
- Location
- Chr X83,999,684 (GRCh38)
- Highest magnitude
- 1.5Minor
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 21%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (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 8 HapMap populations.
- AverageC;C 13% T;T 77%
- European ancestry (Utah)C;C 8% T;T 79%
- Han Chinese (Beijing)C;C 36% T;T 42%
- Japanese (Tokyo)C;C 48% T;T 32%
- Yoruba (Nigeria)C;C 2% T;T 95%
- African ancestry (Southwest US)C;C 2% T;T 89%
- Luhya (Kenya)C;C 4% T;T 92%
- Maasai (Kenya)C;C 5% T;T 90%
- TuscanC;C 2% T;T 96%
Related
Conditions, medicines and genes
Genosets
Genosets combine several genotypes. Twofold checks them in your report.
Notes
From SNPedia
Notes
23andMe blog females with one copy of rs5968255(C) progressed from HIV infection to AIDS more slowly with an average of eight years, nearly four times more than females with no copies or males. The search for host genetic factors of HIV/AIDS pathogenesis in the post-genome era: progress to date and new avenues for discovery. Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations? HIV Progression
Source and license
Adapted from rs5968255 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.