HNMT - NGS including CNV analysis Centogene AG - the Rare Disease Company
Germany | 2 | 1 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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Asthma, susceptibility to, 600807, Autosomal dominant (SCGB3A2 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Asthma, protection against, 600807, Autosomal dominant (MUC7 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Asthma, susceptibility to, 600807, Autosomal dominant (HLA-G gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Asthma, nocturnal, susceptibility to, 600807, Autosomal dominant (ADRB2 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Beta-2-adrenoreceptor agonist, reduced response to (ADRB2 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Asthma, susceptibility to, 600807, Autosomal dominant (IL13 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Asthma, susceptibility to, 600807, Autosomal dominant (PLA2G7 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Asthma, susceptibility to, 600807, Autosomal dominant (TNF gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Asthma, susceptibility to, 600807, Autosomal dominant (CCL11 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Asthma, diminished response to antileukotriene treatment in, 600807, Autosomal dominant (ALOX5 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Atherosclerosis, susceptibility to (ALOX5 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Asthma, susceptibility to, 600807, Autosomal dominant (HNMT gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Asthma, 600807, Autosomal dominant (PHF11 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Mental retardation, autosomal recessive 51, 616739, Autosomal recessive; MRT51 (Autosomal recessive non-syndromic intellectual disability) (HNMT gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Pharmacogenetic panel MVZ diagnosticum Frankfurt MVZ diagnosticum GmbH
Germany | 46 | 29 | - T Targeted variant analysis
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SCGB1A1 Single Gene Fulgent Genetics
United States | 1 | 1 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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SCGB3A2 Single Gene Fulgent Genetics
United States | 1 | 1 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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ALOX5 Single Gene Fulgent Genetics
United States | 1 | 1 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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TNF Single Gene Fulgent Genetics
United States | 3 | 1 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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