Genetic Tests
GENETIC COELIAC DISEASE
€135
Genotyping for HLA-DQ2.2, HLA-DQ2.5, and HLA-DQ8, markers positive in up to 99.7% of all CD patients.
Turn Around Time: 7 days
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HLA haplotypes for coeliac disease should be tested in individuals exhibiting symptoms such as chronic diarrhoea, abdominal pain, bloating, fatigue, as well as those with a family history of the disease.
GENETIC LACTOSE INTOLERANCE
€135
C13910T and G22018A SNPs of the MCM6 gene associated with lactose intolerance.
Turn Around Time: 7 days
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When patient experiences gastrointestinal issues after eating products containing lactose.
GENETIC HAEOCHROMATOSIS
€120
Genotyping (by RT-PCR) of 3 SNPs within the HFE gene, commonly associated with increased risk of developing haemochromatosis: C282Y, H63D and S65C.
Turn Around Time: 7 days
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Patients of north European ancestry with unexplained raised serum Ferritin and random Tsat (>300 lg/l and >50% males; >200 lg/l and >40% females).
MICROBIOME TESTING
€285
In depth analysis of the gut microbiome, identifying over 30 biomarkers that play major roles in the health of the human gut microbiome.
Turn Around Time: 3-4 weeks
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Request to provide rcommendations to changes in diet that can be made to obtain a healthy gut microbiome or when experiencing gastrointestinal issues. Testing includes: overall gut diversity, 15 probiotic biomarkers, 9 potentially harmful bacteria, gut parasites, fungi, archaea, and viruses.
NUTRITION AND LIFESTYLE DNA
€270
Helping you prevent lifestyle diseaes and to avoid nutrirional deficiencies with 40 Genetic markers to keep you performing to your athletic potential.
Turn Around Time: 6 weeks
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Request to optimise personalised nutritional/performance programmes or when nutritional deficiencies are detected.
GENETIC BOWEL CANCER
€720
Screens and detects genetic variants in 11 genes which may increase risk of bowel cancer/Lynch Syndrome.
Turn Around TIme: 6 weeks
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To be requested where the patient has been diagnosed with bowel cancer/Lynch-related cancer or where there is a family history of bowel cancer or Lynch Syndrome.
GENETIC BREAST & OVARIAN CANCER
€720
Screens and detects genetic variants in 8 genes which may increase risk of breast and ovarian cancer.
Turn Around Time: 6 weeks
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Patient has been diagnosed with breast or ovarian cancer, where there is a family history of breast or ovarian cancer, or where there is Ashkenazi Jewish ancestry.
PROSTATE CANCER RISK
€720
Screens and detects genetic variants in 14 genes which may increase risk of prostate cancer.
Turn Around Time: 6 weels
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To be requested where the patient has been diagnosed with prostate cancer, where there is a family history of prostatem cancer, or where there is Ashkenazi Jewish ancestry.
GENETIC FAMILIAL HYPERCHOLESTEROLAEMIA RISK
€750
Screens and detects genetic variants in 5 genes which may increase risk of FH.
Turn Around Time: 6 weeks
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Adults with unexplained total cholesterol of >7.5mmol/l or LDL-C >4.9 mmol/l and 1st/2nd degree relative with history of premature MI.
GENETIC CORE CANCER RISK
€1185
Comprehensively screens and detectsgenetic variants in 29 genes whichmay increase risk of common cancers.
Turn Around Time: 6 weeks
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o be requested where the patient has been diagnosed with cancer, where there is a family history of common cancer types, where no previous variants were detected on a smaller gene panel, or where there is family history of a variant within one of the included genes.
GENETIC FULL CANCER RISK
€1125
Comprehensively screens and detects genetic variants in 94 genes which may increase risk of both common and rare cancers.
Turn Around Time: 6 weeks
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To be requested where the patient has been diagnosed with cancer, where there is a family history of common/rare cancer types, where no previous variants were detected on a smaller gene panel, or where there is family history of a variant within one of the included genes.
GENETIC FULL CARDIAC RISK
€1125
This NGS deep sequencing screen offers a cost-effective way to identify over 100 different genetic variants that cause Inherited Cardiac Conditions.
Turn Around Time: 6 weeks
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When evaluating patients with suspected or confirmed inherited cardiac conditions (ICCs). It is particularly useful for individuals with a family history of cardiac conditions, those presenting with unexplained cardiac symptoms, or in cases where the genetic basis of the condition is unclear.