rs6504649
A SNP in the XYLT2 gene on chromosome 17. Its most notable genotype is C;C: common in clinvar
- Gene
- XYLT2
- Location
- Chr 1750,360,095 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 27%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C), (C;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageC;C 63% C;G 30%
- European ancestry (Utah)C;C 44% C;G 36%
- Han Chinese (Beijing)C;C 69% C;G 29%
- Japanese (Tokyo)C;C 75% C;G 23%
- Yoruba (Nigeria)C;C 65% C;G 32%
Source and license
Adapted from rs6504649 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.