rs187715
A SNP in the SLC6A2 gene on chromosome 16. Its most notable genotype is T;T.
- Gene
- SLC6A2
- Location
- Chr 1655,670,130 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 3%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs187715 on the minus strand: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 8 HapMap populations.
- AverageT;T 96%
- European ancestry (Utah)T;T 90%
- Han Chinese (Beijing)T;T 100%
- Japanese (Tokyo)T;T 100%
- Yoruba (Nigeria)T;T 100%
- African ancestry (Southwest US)T;T 97%
- Gujarati IndianT;T 99%
- Mexican ancestry (Los Angeles)T;T 98%
- TuscanT;T 84%
Related
Other SLC6A2 SNPs
- rs3785143C;Tmay be associated with ADHDMinor
- rs5558A;ANo summary available.Typical
- rs5568A;Acommon in clinvarTypical
- rs5569G;Gcommon in clinvarTypical
- rs734980A;Acommon in complete genomicsTypical
- rs998424G;Gcommon in clinvarTypical
- rs2242446C;Ccommon in clinvarTypical
- rs3785152C;Ccommon in complete genomicsTypical
Source and license
Adapted from rs187715 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.