rs549625604
A SNP in the BBS10 gene on chromosome 12. Its most notable genotype is -;A: Carrier of a Bardet-Biedl syndrome mutation
- Gene
- BBS10
- Location
- Chr 1276,347,713 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- -;-Goodcommon in clinvar
- -;AMost notableBadCarrier of a Bardet-Biedl syndrome mutation
On SNPedia: (-;-), (-;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Notes
From SNPedia
Notes
BBS10 c.271dupT In at least one study, this variant was found to be most common BBS10 gene mutation associated with Bardet-Biedl syndrome in Europeans.
-;A
Unaffected in absence of a second BBS10 gene mutation; see text and links on main rs-page
Source and license
Adapted from rs549625604 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.