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myDNA

myDNA Consumer Pack

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Overview The myDNA test is a Functional Pathology test that analyses the DNA of an individual patient and Pharmacogenomics. myDNA test is the study of how ge…
SKU: 672206
Availability: Out of Stock
$63.10
$61.25
SAVE $1.85

Overview

The myDNA test is a Functional Pathology test that analyses the DNA of an individual patient and Pharmacogenomics. myDNA test is the study of how genetic factors may influence an individual’s response to certain medications. myDNA test combines the study of pharmacology (the study of how drugs work in the body) and genomics (the study of genes and their functions). myDNA test is a reliable way of assisting practitioners in selecting safe and effective medications for their patients based on each patient’s unique genetic makeup.
There are certain genes that contain instructions to build enzymes which, in turn, helps the body to break down medications, primarily in the liver. Every individual’s genetic makeup comprises of variations of each of these protein producing genes. Each gene will also present varying levels of activity (e.g. slow, normal, or fast), and as a result, individuals vary in how slow or fast they break down and clear medications from their body. This test can aid in the clinical understanding of a patient's predisposition to metabolize. This test can help to pinpoint areas in phase I detoxification that may need support.

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myDNA Consumer Pack

$63.10
$61.25
SAVE $1.85

Description

Overview

The myDNA test is a Functional Pathology test that analyses the DNA of an individual patient and Pharmacogenomics. myDNA test is the study of how genetic factors may influence an individual’s response to certain medications. myDNA test combines the study of pharmacology (the study of how drugs work in the body) and genomics (the study of genes and their functions). myDNA test is a reliable way of assisting practitioners in selecting safe and effective medications for their patients based on each patient’s unique genetic makeup.
There are certain genes that contain instructions to build enzymes which, in turn, helps the body to break down medications, primarily in the liver. Every individual’s genetic makeup comprises of variations of each of these protein producing genes. Each gene will also present varying levels of activity (e.g. slow, normal, or fast), and as a result, individuals vary in how slow or fast they break down and clear medications from their body. This test can aid in the clinical understanding of a patient's predisposition to metabolize. This test can help to pinpoint areas in phase I detoxification that may need support.

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