Vitamin B12 metabolism
Testing selected FUT2 variants provides information about genetic factors associated with vitamin B12 levels and is one element of a broader assessment of its metabolism.
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Testing selected FUT2 variants provides information about genetic factors associated with vitamin B12 levels and is one element of a broader assessment of its metabolism.
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This test examines selected CYP2R1 and GC variants associated with vitamin D metabolism and transport, providing information about their genetic background.
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Testing selected TMPRSS6 variants provides information about genetic factors involved in iron regulation. It may form part of investigations chosen for the clinical situation.
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Testing selected GSTT1 variants provides genetic information considered in the context of vitamin C metabolism.
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Analysis of selected HLA variants provides information about genetic predisposition relevant to the assessment of coeliac disease.
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This test provides information about genetic factors associated with primary reduction in lactase activity with age.
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Testing selected ALDOB variants provides information relevant to the assessment of hereditary fructose intolerance.
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Testing selected MTHFR variants provides information about the genetic background of folate metabolism.
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Testing selected CYP1A2 variants provides information about genetic factors involved in caffeine metabolism.
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Testing selected HLA-DRA variants provides genetic information considered in research on susceptibility to peanut allergy.
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Analysis of selected COL5A1 and SOD2 variants provides information considered in the context of tissue function and susceptibility to injury.
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This test provides information about selected ACTN3, NOS3, IL6 and AGT variants considered in the context of exercise physiology.
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Testing selected AVPR1A variants provides information about markers studied in the context of musical traits.
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Testing selected SPOCK1 variants provides information about markers studied in the context of mathematical abilities.
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Analysis of selected KIAA0319 and DCDC2 variants provides information considered in research on susceptibility to dyslexia.
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Testing selected APOE variants provides information about genetic factors involved in lipid metabolism.
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Testing selected COMT and OXTR variants provides information about markers studied in the context of responses to stress.
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Analysis of selected APOE and TREM2 variants provides information considered in the assessment of susceptibility to Alzheimer's disease.
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Testing selected SNCA variants provides genetic information relevant to the assessment of susceptibility to Parkinson's disease.
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Testing selected CDKAL1 variants provides information about genetic markers associated with susceptibility to type 2 diabetes.
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Analysis of selected FTO variants provides information about genetic factors associated with body weight.
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Testing selected ACE and NOS3 variants provides information about markers considered in blood pressure regulation. It concerns susceptibility rather than a current blood pressure r...
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Testing selected LPA and AGT variants provides information about genetic factors associated with lipid metabolism and cardiovascular regulation.
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Testing selected PRSS1 and SPINK1 variants provides information relevant to inherited pancreatic conditions, particularly those associated with pancreatitis.
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Testing selected BRCA1 and BRCA2 variants provides information that may be relevant to inherited predisposition to breast and ovarian cancer.
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Analysis of selected variants associated with inherited susceptibility to colorectal cancer provides genetic information within the specified test scope.
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Testing selected HOXB13 and CHEK2 variants provides information considered in the assessment of inherited susceptibility to prostate cancer.
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Testing selected MC1R and CDKN2A variants provides information about pigmentation and selected inherited factors associated with melanoma susceptibility.
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Testing selected CHRNA3 and CDKN1A variants provides information about markers described in studies of susceptibility to lung cancer.
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Testing HLA markers associated with psoriasis provides genetic information considered in the assessment of susceptibility to this condition.
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Testing selected AR and HDAC4 variants provides information about markers studied in the genetic background of androgenetic alopecia.
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This test identifies a specified F5 variant associated with an inherited tendency to venous thromboembolism.
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Testing the prothrombin gene F2 identifies a specified variant considered in the assessment of inherited susceptibility to venous thrombosis.
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FVR2 testing concerns a selected variant or R2 haplotype within F5. It provides genotype information distinct from Factor V Leiden testing.
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PAI-1 testing provides information about a selected genetic polymorphism associated with regulation of fibrinolysis, the process of dissolving a blood clot.
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Testing selected CD36 variants provides information about markers described in the context of lipid transport and vitamin E metabolism.
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Testing selected AQP3 variants provides information about genetic markers associated with skin barrier function and cellular water transport.
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This test examines a human genetic variant described in population studies of COVID-19 severity. It provides genotype information rather than detecting the virus.
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Testing selected MMP1 and MMP3 variants provides information about markers associated with extracellular matrix remodelling relevant to skin structure.
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Testing selected ASIP variants provides information about genetic markers associated with pigmentation and aspects of the skin's response to sunlight.
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Testing selected CAT and SOD2 variants provides information about markers associated with cellular protection against oxidative stress.
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Testing selected FLG variants provides information about changes in the filaggrin gene, which is important for the epidermal barrier.
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Testing selected FN3K and ALG6 variants provides information about markers described in the context of sugar metabolism and processes associated with skin ageing.
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