rs2223841
A SNP on chromosome X. Its most notable genotype is C;C: less likely to go bald
- Gene
- None listed
- Location
- Chr X67,350,329 (GRCh38)
- Highest magnitude
- 2.1Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 30%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2223841 on the minus strand: (A;A), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 7 HapMap populations.
- AverageT;T 62% C;C 32%
- European ancestry (Utah)T;T 69% C;C 11%
- Han Chinese (Beijing)T;T 100% C;C 0%
- Japanese (Tokyo)T;T 100% C;C 0%
- Yoruba (Nigeria)T;T 0% C;C 100%
- Luhya (Kenya)T;T 2% C;C 94%
- Mexican ancestry (Los Angeles)T;T 84% C;C 7%
- TuscanT;T 77% C;C 14%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
male-pattern baldness. Full text available. *G less likely to go bald before age 40 *A more likely to go bald before age 40
T;T
more likely to go bald before age 40
C;C
less likely to experience baldness before age 40
Source and license
Adapted from rs2223841 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.