rs777923890

A SNP in the PSEN1 gene on chromosome 14. Its most notable genotype is C;T: Early onset Alzheimer's association specifically in African-Americans?

Gene
PSEN1
Location
Chr 1473,173,727 (GRCh38)
Highest magnitude
7.0Very important
Tested on
Not on consumer chips

Genotypes

As shown in 23andMe and AncestryDNA files.

On SNPedia: (C;C), (C;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Conditions, medicines and genes

Notes

From SNPedia

Notes

rs777923890 represents a rare mutation within an intron of the PSEN1 gene on chromosome 14. A relatively small study published early 2017 hypothesized that the rs777923890(T) allele may be associated with early-onset Alzheimer's disease specifically in African-Americans.

C;T

see discussion at rs777923890

Source and license

Adapted from rs777923890 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.