rs111033560

A SNP in the CEP85L gene on chromosome 6. Its most notable genotype is G;T: Familial hypertrophic cardiomyopathy (possible)

Gene
CEP85L
Location
Chr 6118,559,037 (GRCh38)
Highest magnitude
6.0Very important
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. G;TMost notableBadFamilial hypertrophic cardiomyopathy (possible)Very important · 6.0
  2. T;TGoodcommon in clinvarTypical · 0.0

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

Conditions, medicines and genes

Other CEP85L SNPs

All CEP85L SNPs

Notes

From SNPedia

Notes

The rare minor allele of this variant is reported to be pathogenic/likely pathogenic for familial hypertrophic cardiomyopathy (HCM), according to .

G;T

see discussion at rs111033560

Source and license

Adapted from rs111033560 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.