rs869025212
A SNP in the BAP1 gene on chromosome 3. Its most notable genotype is -;G: BAP1 Tumor Predisposition Syndrome
- Gene
- BAP1
- Location
- Chr 352,403,428 (GRCh38)
- Highest magnitude
- 6.0Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- -;GMost notableBadBAP1 Tumor Predisposition Syndrome
- G;GGoodcommon in clinvar
- I;IGoodcommon genotype
SNPedia records rs869025212 on the minus strand: (-;C), (C;C), (I;I). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Other BAP1 SNPs
- rs375129361C;TBAP1 Tumor Predisposition SyndromeVery important
- rs387906848A;GBAP1 Tumor Predisposition SyndromeVery important
- rs397509413-;CBAP1 Tumor Predisposition SyndromeVery important
- rs397509414-;CBAP1 Tumor Predisposition SyndromeVery important
- rs774730309A;GBAP1 Tumor Predisposition SyndromeVery important
- rs864622592A;GBAP1 Tumor Predisposition SyndromeVery important
- rs869312757A;GBAP1 Tumor Predisposition SyndromeVery important
Notes
From SNPedia
Notes
aka c.1717delC and p.Leu573Trpfs See BAP1 tumor predisposition syndrome
Source and license
Adapted from rs869025212 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.