rs375129361

A SNP in the BAP1 gene on chromosome 3. Its most notable genotype is C;T: BAP1 Tumor Predisposition Syndrome

Gene
BAP1
Location
Chr 352,408,056 (GRCh38)
Highest magnitude
6.0Very important
Tested on
23andMe, AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;TMost notableBadBAP1 Tumor Predisposition SyndromeVery important · 6.0
  2. T;TGoodcommon in clinvarTypical · 0.0

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

Other BAP1 SNPs

All BAP1 SNPs

Source and license

Adapted from rs375129361 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.