{"product_id":"egtargens","title":"Single Gene analysis(Sequencing only)","description":"\u003cp\u003etest is designed to analyze the complete coding regions and intron–exon boundaries of a single gene using next-generation sequencing (NGS) or Sanger sequencing, depending on the gene and clinical indication. This test focuses exclusively on sequencing analysis and does not include deletion or duplication (copy number) analysis.\u003c\/p\u003e\u003cp\u003eThis test is particularly useful when the patient’s clinical presentation, family history, or biochemical findings strongly suggest the involvement of a specific gene known to be associated with the phenotype. By targeting a single, well-defined gene, this approach provides a cost-effective and precise method for identifying single nucleotide variants (SNVs), small insertions, or small deletions that may be pathogenic.\u003c\/p\u003e","brand":"Enigma Genomics","offers":[{"title":"Default Title","offer_id":60790448488734,"sku":"EGTARGENS","price":1000.0,"currency_code":"SAR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/6678\/6590\/files\/enigma-test-icon-targeted-target-v1.png?v=1793571419","url":"https:\/\/shop.enigmagenomics.com\/en\/products\/egtargens","provider":"Enigma Genomics","version":"1.0","type":"link"}