rs111033571

A SNP in the TRIM32 gene on chromosome 9. Its most notable genotype is T;T: Bardet-Biedl syndrome 11 (reported)

Gene
TRIM32
Location
Chr 9116,698,130 (GRCh38)
Highest magnitude
5.0Very important
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CGoodcommon in clinvarTypical · 0.0
  2. C;TBadCarrier of a Bardet-Biedl syndrome mutationImportant · 3.0
  3. T;TMost notableBadBardet-Biedl syndrome 11 (reported)Very important · 5.0

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

Notes

From SNPedia

Notes

aka c.388C>T (p.Pro130Ser or P130S)

C;T

Unaffected in absence of a second TRIM32 gene mutation

T;T

see text and links via main rs-page

Source and license

Adapted from rs111033571 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.