rs11966200
A SNP in the SLC44A4 gene on chromosome 6. Its most notable genotype is C;C: common on affy axiom data
- Gene
- SLC44A4
- Location
- Chr 631,869,289 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 5%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CMost notableGoodcommon on affy axiom data
- C;TBad1.88x risk of vitiligo
- T;TBad1.88x risk of vitiligo
On SNPedia: (C;C), (C;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.
- AverageC;C 89% C;T 11% T;T <1%
- European ancestry (Utah)C;C 97% C;T 4% T;T 0%
- Han Chinese (Beijing)C;C 92% C;T 8% T;T 0%
- Japanese (Tokyo)C;C 98% C;T 2% T;T 0%
- Yoruba (Nigeria)C;C 81% C;T 19% T;T 0%
- African ancestry (Southwest US)C;C 74% C;T 26% T;T 0%
- Chinese (Denver)C;C 95% C;T 6% T;T 0%
- Gujarati IndianC;C 98% C;T 2% T;T 0%
- Luhya (Kenya)C;C 79% C;T 20% T;T <1%
- Mexican ancestry (Los Angeles)C;C 91% C;T 9% T;T 0%
- Maasai (Kenya)C;C 80% C;T 19% T;T <1%
- TuscanC;C 91% C;T 9% T;T 0%
Related
Source and license
Adapted from rs11966200 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.