rs111033260

A SNP in the PCDH15 gene on chromosome 10. Its most notable genotype is A;A: Usher syndrome Type I

Gene
PCDH15
Location
Chr 1054,317,414 (GRCh38)
Highest magnitude
5.0Very important
Tested on
AncestryDNA

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GGoodcommon in clinvarTypical · 0.0
  2. A;GBadcarrier for Usher syndrome Type I alleleImportant · 3.0
  3. A;AMost notableBadUsher syndrome Type IVery important · 5.0

SNPedia records rs111033260 on the minus strand: (C;C), (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Other PCDH15 SNPs

All PCDH15 SNPs

Source and license

Adapted from rs111033260 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.