import React from 'react';
import Image from 'next/image';
const FeatureCard = ({ icon, title, description }) => (
);
export default function HereditaryCancerPanel() {
const features = [
{
title: "Comprehensive Gene Coverage",
desc: "Includes high- and moderate-risk genes such as BRCA1, BRCA2, TP53, MLH1, MSH2, APC, and others.",
icon: "/images/icons/gene-coverage.png"
},
{
title: "Germline Variant Detection",
desc: "Accurately detects SNVs, Indels, and selected CNVs in genes associated with inherited cancer risk.",
icon: "/images/icons/variant-detection.png"
},
{
title: "Family-Centered Testing",
desc: "Supports cascade testing for at-risk relatives, enabling early detection and prevention.",
icon: "/images/icons/family-centered-testing.png"
},
{
title: "Clinical Actionability",
desc: "Provides insights that guide surveillance, preventive measures, and personalized treatment planning.",
icon: "/images/icons/clinical-actionability.png"
},
{
title: "High Sensitivity & Specificity",
desc: "Uses ≥100X sequencing depth with ≥90% Q30 base quality for reliable variant calling.",
icon: "/images/icons/high-sensitivity-specificity.png"
},
{
title: "Expert Interpretation & Reporting",
desc: "Variants classified using ACMG guidelines, backed by curated literature and clinical databases.",
icon: "/images/icons/expert-interpretation-reporting.png"
}
];
const points = [
"About 5-10% of all cancers are linked to inherited genetic mutations, often going undetected until late stages or after multiple family members are affected.",
"The Operify Hereditary Cancer Panel screens key high- and moderate-risk genes associated with hereditary cancer syndromes like HBOC, Lynch Syndrome (LS), Li Fraumeni Syndrome (LFS), Familial Adenomatous Polyposis (FAP), Cowden Syndrome (CS), Peutz-Jeghers Syndrome (PJS), Neurofibromatosis (NF) etc.",
"Early identification of germline mutations enables proactive clinical decisions, including risk-reducing strategies, targeted surveillance, and family cascade testing.",
"Studies show that genetic testing in hereditary cancer cases improves outcomes and informs care for both patients and at-risk relatives."
];
return (
Operify Hereditary Cancer Panel
{points.map((point, idx) => (
-
{point}
))}
Key Features
{features.map((feature, index) => (
))}
);
}