export default function CancerKeyFeatures() { const features = [ { title: "Comprehensive Gene Coverage", desc: "Includes high- and moderate-risk genes such as BRCA1, BRCA2, TP53, MLH1, MSH2, APC, and others." }, { title: "Germline Variant Detection", desc: "Accurately detects SNVs, Indels, and selected CNVs in genes associated with inherited cancer risk." }, { title: "Family-Centered Testing", desc: "Supports cascade testing for at-risk relatives, enabling early detection and prevention." }, { title: "Clinical Actionability", desc: "Provides insights that guide surveillance, preventive measures, and personalized treatment planning." }, { title: "High Sensitivity & Specificity", desc: "Uses ≥100X sequencing depth with ≥90% Q30 base quality for reliable variant calling." }, { title: "Expert Interpretation & Reporting", desc: "Variants classified using ACMG guidelines, backed by curated literature and clinical databases." }, { title: "Genetic Counseling Support", desc: "Optional access to pre- and post-test counseling for patient education and informed decision-making." } ]; return (

Key Features

{features.map((f, idx) => (

{f.title}

{f.desc}

))}
); }