rs821616
A SNP in the TSNAX-DISC1 gene on chromosome 1. Its most notable genotype is T;T: cognitive decline in older women
- Gene
- TSNAX-DISC1
- Location
- Chr 1232,008,852 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 25%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs821616 on the minus strand: (A;A), (A;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 4 HapMap populations.
- AverageT;T 7% A;T 32% A;A 61%
- European ancestry (Utah)T;T 14% A;T 39% A;A 48%
- Han Chinese (Beijing)T;T 2% A;T 24% A;A 73%
- Japanese (Tokyo)T;T 2% A;T 9% A;A 89%
- Yoruba (Nigeria)T;T 11% A;T 56% A;A 33%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
Women with two rs821616(T) SNPs seem to experience more rapid cognitive decline as they age compared to men. 13 single-nucleotide polymorphisms (SNPs) in 723 members of 179 Finnish Bipolar disorder families. *rs821616 verbal fluency
Source and license
Adapted from rs821616 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.