rs2073724
A SNP in the TCF19 gene on chromosome 6. Its most notable genotype is C;T: Higher (1.9x) risk for COVID-19 illness being severe
- Gene
- TCF19
- Location
- Chr 631,161,930 (GRCh38)
- Highest magnitude
- 1.9Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 9%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon on affy axiom data
- C;TMost notableBadHigher (1.9x) risk for COVID-19 illness being severe
On SNPedia: (C;C), (C;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 86% C;T 13%
- European ancestry (Utah)C;C 87% C;T 12%
- Han Chinese (Beijing)C;C 86% C;T 12%
- Japanese (Tokyo)C;C 96% C;T 4%
- Yoruba (Nigeria)C;C 82% C;T 18%
- African ancestry (Southwest US)C;C 93% C;T 7%
- Chinese (Denver)C;C 92% C;T 8%
- Gujarati IndianC;C 81% C;T 18%
- Luhya (Kenya)C;C 90% C;T 10%
- Mexican ancestry (Los Angeles)C;C 72% C;T 26%
- Maasai (Kenya)C;C 96% C;T 4%
- TuscanC;C 75% C;T 24%
Notes
From SNPedia
Notes
Distinct genetic loci control plasma HIV-RNA and cellular HIV-DNA levels in HIV-1 infection: the ANRS Genome Wide Association 01 study.
C;T
see rs143334143
Source and license
Adapted from rs2073724 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.