rs8099917
A SNP on chromosome 19. Its most notable genotype is G;G: lower odds of responding to PEG-IFNalpha/RBV treatment
- Gene
- None listed
- Location
- Chr 1939,252,525 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 14%
Genotypes
As shown in 23andMe and AncestryDNA files.
- G;GMost notableBadlower odds of responding to PEG-IFNalpha/RBV treatment
- G;TBadModerately lower odds of responding to PEG-IFNalpha/RBV treatment
- T;TGoodcommon
On SNPedia: (G;G), (G;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.
- AverageG;G 2% G;T 22% T;T 76%
- European ancestry (Utah)G;G 3% G;T 25% T;T 73%
- Han Chinese (Beijing)G;G 0% G;T 12% T;T 88%
- Japanese (Tokyo)G;G <1% G;T 20% T;T 79%
- Yoruba (Nigeria)G;G <1% G;T 3% T;T 96%
- African ancestry (Southwest US)G;G 0% G;T 19% T;T 81%
- Chinese (Denver)G;G <1% G;T 11% T;T 88%
- Gujarati IndianG;G 2% G;T 33% T;T 65%
- Luhya (Kenya)G;G 0% G;T 12% T;T 88%
- Mexican ancestry (Los Angeles)G;G 9% G;T 47% T;T 45%
- Maasai (Kenya)G;G 1% G;T 20% T;T 79%
- TuscanG;G 1% G;T 40% T;T 59%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
23andMe blog rs8099917(C) less likely to respond to Hepatitis C treatment. rs12979860(C;C) better able to become naturally Hepatitis C virus-free. rs12980275(A) usually corresponds to the rs12979860(C)
G;G
Substantially lower odds of responding to PEG-IFNalpha/RBV treatment for hepatitis C.
G;T
Moderately lower odds of responding to PEG-IFNalpha/RBV treatment for hepatitis C.
Source and license
Adapted from rs8099917 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.