Explaining Results in the PGx report: Heterozygous Genotypes

Explaining Results in the PGx report: Heterozygous Genotypes

Written by: Jamie Fernandez, B.Sc Honours in Genetics, Content Specialist

 

Short recap: 

As you may know from our previous articles, your DNA is a code like binary code, but instead of 1’s and 0’s, DNA is made up of A’s, T’s, C’s and G’s. These are called nucleotides. For the most part, our codes are the same; however, there are points along the DNA where the code is highly variable from person to person. These points are called single nucleotide polymorphisms (SNPs), which contribute to making us unique. Additionally, you receive two sets of DNA (to be more precise two sets of chromosomes), one from each parent, and so for each SNP, there are two corresponding letters (we can also call them alleles). This combination of letters (alleles) is called a genotype. Some of these SNPs determine how you may metabolize drugs and thus forms the basis of pharmacogenetic testing. For more, please explore the articles in our Genetic 101 section. 

Genotypes can be homozygous or heterozygous. A homozygous genotype is when the two alleles are the same, for example TT or CC. A heterozygous genotype is when the who alleles are different, for example AT or CA. You may have noticed that in the case of heterozygous genotypes, the order in which they are written sometimes differs.

 explaining results in the PGx report

In the above, both genotypes contain an A and a G; however, they are written differently in each case. You may be wondering: Is there a difference between writing it the genotype as AG or GA? No, there is no difference. Regardless of the order in which it is written, the genotype is the same. In both the above examples, at both these SNPs, there is an A in one set of the DNA there is an A, and the other set contains a G. It makes no difference whether the A is the maternal set of DNA and the G in the paternal set or visa versa. 

So, why do we write them differently if they are the same? 

The order depends on which allele is the allele that is reported in the human reference genome as the reference (REF) allele. The other allele is known as the alternative (ALT) allele. It is common practice that the reference allele is written first, and the alternative allele is written second. 

Conclusion 

The main take home message here is that you do not have to worry about the order in which heterozygous genotype are written. We suggest that you rather focus on reading the annotation text to asses the pharmacological impact associated with your genotype. 

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