rs869312829
A SNP in the SETD1A gene on chromosome 16. Its most notable genotype is A;G: Possible association with schizophrenia
- Gene
- SETD1A
- Location
- Chr 1630,963,431 (GRCh38)
- Highest magnitude
- 3.5Important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AGoodcommon in clinvar
- A;GMost notableBadPossible association with schizophrenia
On SNPedia: (A;A), (A;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Notes
From SNPedia
Notes
also known as c.518-2A>G Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
A;G
See text and links via main rs-page
Source and license
Adapted from rs869312829 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.