rs143332484
A SNP in the LOC105375056 gene on chromosome 6. Its most notable genotype is C;T: Moderate increase (1.67x) in risk for Alzheimer's disease
- Gene
- LOC105375056
- Location
- Chr 641,161,469 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon/normal
- C;TMost notableBadModerate increase (1.67x) in risk for Alzheimer's disease
- T;TBadModerate increase (1.67x) in risk for Alzheimer's disease
On SNPedia: (C;C), (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs143332484 (p.Arg62His) is a risk variant for Alzheimer's disease found in the TREM2 gene (P = 1.55 × 10-14, OR = 1.67). This gene is highly expressed in microglia which are known to interact with the immune system in AD.
C;T
see rs143332484
T;T
see rs143332484
Source and license
Adapted from rs143332484 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.