rs683395
A SNP in the LAMP3 gene on chromosome 3. Its most notable genotype is T;T.
- Gene
- LAMP3
- Location
- Chr 3183,152,030 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 12%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs683395 on the minus strand: (A;A), (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.
- AverageT;T 0% G;G 2% A;G 22% A;A 76%
- European ancestry (Utah)T;T 0% G;G 0% A;G 19% A;A 81%
- Han Chinese (Beijing)T;T 0% G;G 3% A;G 18% A;A 80%
- Japanese (Tokyo)T;T 0% G;G <1% A;G 19% A;A 81%
- Yoruba (Nigeria)T;T 0% G;G 6% A;G 29% A;A 65%
- African ancestry (Southwest US)T;T 0% G;G 0% A;G 32% A;A 68%
- Chinese (Denver)T;T 0% G;G 2% A;G 16% A;A 83%
- Gujarati IndianT;T 0% G;G 0% A;G 16% A;A 84%
- Luhya (Kenya)T;T 0% G;G 6% A;G 26% A;A 69%
- Mexican ancestry (Los Angeles)T;T 0% G;G 0% A;G 12% A;A 88%
- Maasai (Kenya)T;T 0% G;G 8% A;G 42% A;A 50%
- TuscanT;T 0% G;G 0% A;G 15% A;A 85%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs683395 has been reported in a large study to be associated with bipolar disorder. The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.47 (CI 1.26-1.71), and for homozygotes, 1.3 (CI 0.69-2.46). Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort.
Source and license
Adapted from rs683395 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.