rs397509414
A SNP in the BAP1 gene on chromosome 3. Its most notable genotype is -;C: BAP1 Tumor Predisposition Syndrome
- Gene
- BAP1
- Location
- Chr 352,403,491 (GRCh38)
- Highest magnitude
- 6.0Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- -;CMost notableBadBAP1 Tumor Predisposition Syndrome
- C;CGoodcommon in clinvar
SNPedia records rs397509414 on the minus strand: (-;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other BAP1 SNPs
- rs375129361C;TBAP1 Tumor Predisposition SyndromeVery important
- rs387906848A;GBAP1 Tumor Predisposition SyndromeVery important
- rs397509413-;CBAP1 Tumor Predisposition SyndromeVery important
- rs774730309A;GBAP1 Tumor Predisposition SyndromeVery important
- rs864622592A;GBAP1 Tumor Predisposition SyndromeVery important
- rs869025212-;GBAP1 Tumor Predisposition SyndromeVery important
- rs869312757A;GBAP1 Tumor Predisposition SyndromeVery important
Source and license
Adapted from rs397509414 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.