rs770913157

A SNP in the SETD1A gene on chromosome 16. Its most notable genotype is C;T: Possible association with schizophrenia

Gene
SETD1A
Location
Chr 1630,965,819 (GRCh38)
Highest magnitude
3.5Important
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CGoodcommon in clinvarTypical · 0.0
  2. C;TMost notableBadPossible association with schizophreniaImportant · 3.5

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

Other SETD1A SNPs

All SETD1A SNPs

Notes

From SNPedia

Notes

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. referred to in the cited paper as 16:30977140_C/G and also as p.Y646X

C;T

See text and links via main rs-page

Source and license

Adapted from rs770913157 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.