rs3077
A SNP in the HLA-DPA1 gene on chromosome 6. Its most notable genotype is G;G: 1.8 times higher odds of having chronic hepatitis B
- Gene
- HLA-DPA1
- Location
- Chr 633,065,245 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 40%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GMost notableBad1.8 times higher odds of having chronic hepatitis B
- A;AGoodcommon in complete genomics
SNPedia records rs3077 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 11 HapMap populations.
- AverageG;G 24% A;A 36%
- European ancestry (Utah)G;G 4% A;A 73%
- Han Chinese (Beijing)G;G 36% A;A 10%
- Japanese (Tokyo)G;G 43% A;A 21%
- Yoruba (Nigeria)G;G 54% A;A 8%
- African ancestry (Southwest US)G;G 23% A;A 30%
- Chinese (Denver)G;G 48% A;A 9%
- Gujarati IndianG;G 14% A;A 43%
- Luhya (Kenya)G;G 23% A;A 33%
- Mexican ancestry (Los Angeles)G;G 3% A;A 62%
- Maasai (Kenya)G;G 8% A;A 47%
- TuscanG;G 5% A;A 61%
Related
Notes
From SNPedia
Notes
23andMe blog rs3077(A) and rs9277535(A) may reduce risk of Hepatitis B infection The textile plot: a new linkage disequilibrium display of multiple-single nucleotide polymorphism genotype data. Non-invasive screening of HLA-DPA1 and HLA-DPB1 alleles for persistent hepatitis B virus infection: susceptibility for vertical transmission and toward a personalized approach for vaccination and treatment. A common HLA-DPA1 variant is a major determinant of hepatitis B virus clearance in Han Chinese. Evaluation of genetic susceptibility loci for chronic hepatitis B in Chinese: two independent case-control studies.
G;G
1.8 times higher odds of having chronic hepatitis B
A;A
lower risk of hepatitis B
Source and license
Adapted from rs3077 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.