rs35152987
A SNP in the HBD gene on chromosome 11. Its most notable genotype is C;C: common in clinvar
- Gene
- HBD
- Location
- Chr 115,234,352 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- <1%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs35152987 on the minus strand: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in one HapMap population.
- European ancestry (Utah)C;C 99%
Related
Other HBD SNPs
- rs33956485A;Acommon in complete genomicsTypical
- rs33971270G;Gcommon in complete genomicsTypical
- rs34390965C;Ccommon in complete genomicsTypical
- rs34460332C;Ccommon in complete genomicsTypical
- rs34975911A;Acommon in clinvarTypical
- rs35329985C;Ccommon in complete genomicsTypical
- rs35518301T;Tcommon in clinvarTypical
- rs35848600G;Gcommon in complete genomicsTypical
Source and license
Adapted from rs35152987 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.