Select Your Own Genetic Tests

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Select Your Own Genetic Tests

Alpha-1 Antitrypsin (Pi*S & Pi*Z alleles)
R4274,40
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Angelman Syndrome – Methylation-Sensitive MLPA
R6565,20
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Ankylosing spondylitis HLA B27
R1026,00
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Apolipoprotein E PCR (*2, *4 alleles)
R4274,40
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Ataxia Telangiectasia Mutated
R5200,80
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Beckwith-Wiedemann/Russell-Silver Syndrome
R6565,20
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CAH-21 Hydroxylase Congenital Adrenal Hyperplasia
R6565,20
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Cardiofaciocutaneous Syndromes, incl Noonan Syndrome (17 Genes)
R15319,20
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CMT – Charcot-Marie-Tooth Disease
R6565,20
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Cystic Fibrosis: CFTR Gene Seq & MLPA
R11817,60
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DPYD (Dihydropyrimidine Dehydrogenase
R4274,40
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Duchenne/Becker Muscular Dystrophy (DMD/BMD)
R11817,60
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Dystonia – 19 Genes
R18820,80
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Factor II (G20210A; Prothrombin PCR)
R2137,20
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Factor V (R506Q; Factor V Leiden Mutation)
R2137,20
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Familial Hypercholesterolemia Panel – LDLR, PCSK9 and APOB Genes
R8316,00
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Familial Mediterranean Fever – MEFV,MVK, NLRP3, PSTPIP1 and TNFRSF1A Genes
R11817,60
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Fanconi Anaemia – 16 Genes Including FANCA & FANCG
R13568,40
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Fanconi Anaemia – Common SA Black ( FANGC) And Afrikaner (FANCA) Mutations
R8316,00
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Fragile-X (FMR1 Gene)
R4814,40
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Haemochromatosis Genes
R8316,00
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Haemochromatosis HFE (C282Y,H63D,S65C)
R4274,40
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Hereditary Spastic Paraplegia – 21 Genes
R13135,20
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HLA DQ2/DQ8
R2137,20
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HLA-B51
R2137,20
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Huntington Disease
R3063,60
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Interstitial Lung Disease
R15319,20
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Malignant Hyperthermia – 3 Genes (BCHE,CACNAS,RYR1)
R13135,20
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Marfanoid Syndromes
R18820,80
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MODY (Maturity Onset Of Diabetes In Young) – 16 Genes
R13568,40
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MTHFR (C677T; A1298C) Homocysteine
R2137,20
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Neurofibromatosis – 3 Genes (NF1,NF2,SPRED1)
R18820,80
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Porphyria Genes
R8316,00
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Porphyria Variegata (R59W)
R3072,00
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Prader-Willi Syndrome – Methylation-sensitive MLPA
R6565,20
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Primary Ciliary Dyskinesia (PCD)
R15319,20
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Rett Syndrome (MECP2 Gene Sequencing & CNV/MLPA
R6565,20
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Spinal Muscular Atrophy (SMA) – SMN1 & SMN2 Copу Number (MLPA)
R6565,20
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TPMT (*1, *2 & *3 Alleles; Thiopurine methyltransferase)
R4274,40
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