{"product_id":"eggenpren","title":"Prenatal Whole Genome Sequencing","description":"\u003cp\u003eIt provides comprehensive insight into both coding and non-coding regions of the genome, identifying potential single-nucleotide variants (SNVs), insertions\/deletions, structural variants, and copy number variations (CNVs).\u003cbr\u003eThis test is typically performed on samples obtained via amniocentesis or chorionic villus sampling (CVS), and is especially useful in cases where:\u003cbr\u003eRoutine prenatal screening or imaging (e.g., ultrasound) shows abnormalities\u003c\/p\u003e\u003cp\u003eThere’s a history of genetic disorders\u003cbr\u003ePrevious tests (karyotype, microarray) were inconclusive\u003cbr\u003eKey Benefits:\u003cbr\u003eHigh diagnostic yield for unexplained fetal anomalies\u003cbr\u003eDetection of rare genetic disorders\u003cbr\u003eInforms clinical decision-making during pregnancy\u003c\/p\u003e","brand":"Enigma Genomics","offers":[{"title":"Default Title","offer_id":60790442656030,"sku":"EGGENPREN","price":5000.0,"currency_code":"SAR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/6678\/6590\/files\/enigma-test-icon-general-carrier-v1.png?v=1793571522","url":"https:\/\/shop.enigmagenomics.com\/products\/eggenpren","provider":"Enigma Genomics","version":"1.0","type":"link"}