Genetic testing technology wrongly detects the presence of very rare genetic variants

A technology that is widely used by commercial genetic testing companies is "extremely unreliable" in detecting very rare variants, meaning results suggesting individuals carry rare disease-causing genetic variants are usually wrong, according to new research published in the BMJ.

After hearing of cases where women had surgery scheduled after wrongly being told they had very rare genetic variations in the gene BRCA1 that could significantly increase the risk of breast cancer, a team at the University of Exeter conducted a large-scale analysis of the technology using data from nearly 50,000 people.

They found that the technology wrongly identified the presence of very rare genetic variants in the majority of cases.

The team analyzed SNP chips, which test genetic variation at hundreds-of-thousands of specific locations across the genome. While excellent at detecting common genetic variation that can increase the risk of diseases such as type 2 diabetes, geneticists have long known they are less reliable at detecting rarer variation.

However, this problem is less well known outside the genetic research community, and SNP chips are widely used by commercial companies that offer genetic testing directly to consumers.

SNP chips are fantastic at detecting common genetic variants, yet we have to recognize that tests that perform well in one scenario are not necessarily applicable to others. We've confirmed that SNP chips are extremely poor at detecting very rare disease-causing genetic variants, often giving false-positive results that can have a profound clinical impact. These false results had been used to schedule invasive medical procedures that were both unnecessary and unwarranted."

Caroline Wright, Study Senior Author and Professor in Genomic Medicine, University of Exeter Medical School

The team compared data from SNP chips with data from the more reliable tool of next-generation sequencing in 49,908 participants of UK Biobank, and an additional 21 people who shared results of their consumer genetic tests via the Personal Genome Project.

The study concluded that SNP chips performed extremely well in detecting common genetic variants. However, the rarer the variation was, the less reliable the results became.

In very rare variants, present in fewer than 1 in 100,000 individuals, typical of those causing rare genetic disease, 84 percent were false positives in UK Biobank. In the data from commercial customers, 20 of 21 individuals analyzed had at least one false-positive rare disease-causing variant that had been incorrectly genotyped.

Dr. Leigh Jackson, Lecturer in Genomic Medicine at the University of Exeter and co-author of the paper, said: "The number of false positives on rare genetic variants produced by SNP chips was shockingly high. To be clear: a very rare, disease-causing variant detected using an SNP chip is more likely to be wrong than right. Although some consumer genomics companies perform sequencing to validate important results before releasing them to consumers, most consumers also download their "raw" SNP chip data for secondary analysis, and this raw data still contain these incorrect results. The implications of our findings are very simple: SNP chips perform poorly for detecting very rare genetic variants and the results should never be used to guide a patient's medical care unless they have been validated."

Journal reference:

Weedon, M. N., et al. (2021) Use of SNP chips to detect rare pathogenic variants: retrospective, population based diagnostic evaluation. BMJ.


The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
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