rs28936379
A SNP in the PSEN2 gene on chromosome 1. Its most notable genotype is A;G: early-onset Alzheimers disease
- Gene
- PSEN2
- Location
- Chr 1226,888,977 (GRCh38)
- Highest magnitude
- 9.0Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AGoodcommon in clinvar
- A;GMost notableBadearly-onset Alzheimers disease
On SNPedia: (A;A), (A;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Other PSEN2 SNPs
- rs28936380C;Gearly-onset Alzheimer's diseaseVery important
- rs63749851A;CEarly-onset Alzheimer's diseaseVery important
- rs63750215A;Tearly-onset Alzheimer's diseaseVery important
- rs61761208A;TEarly-onset Alzheimer's mutation (reported)Very important
- rs63749884A;Gearly-onset Alzheimer's disease; penetrance not 100%Very important
- rs63750666C;Tearly-onset Alzheimer's disease; penetrance unclearVery important
- rs200754713A;GFrontotemporal dementia (reported)Very important
- rs367855127C;TPossible early-onset Alzheimer's disease mutation; see discussionVery important
Notes
From SNPedia
Notes
rs28936379, also known as c.715A>G, M239V or Met239Val, is a SNP in the presenilin 2 PSEN2 gene. Inherited as an autosomal dominant, the rare rs28936379(G) allele is considered causative for early-onset Alzheimer's disease. This mutation is also reported as pathogenic in ClinVar, AlzForum and listed as "definitely" pathogenic in .
A;G
The rs28936379(G) allele is reported to lead to early-onset Alzheimer's disease.
Source and license
Adapted from rs28936379 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.