Prenatal screening
G-NIPT® Basic
Screening for trisomy 21, 18, and 13; sex chromosome aneuploidies; fetal sex confirmation; and other autosomal trisomies.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- Streck cfDNA tube
- TAT
- ~17 days incl. shipping
Clinical test menu
Tests categorized by clinical use case.
Browse AC testing pathways by indication rather than by laboratory catalog: prenatal screening, oncology, hemato-oncology, hereditary cancer, rare disease, reproductive genetics, preventive genomics, and wellness-oriented tests.
Tests are intended to be ordered and interpreted in consultation with a qualified physician. Turnaround times are quoted end to end — the reference laboratory’s processing time plus courier transit from Jordan, 5 days to Korea and 8 days to the United States. They remain indicative and may vary with specimen quality, shipment timing, and laboratory workflow.
Menu overview
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Prenatal ScreeningPrecision Oncology — Solid TumorHematologic OncologyHereditary CancerRare Disease Genomics
49 tests shown
5 tests
Prenatal Screening
NIPT and non-invasive prenatal screening options from maternal blood.
View clinical information →Prenatal screening
AC-NIP-BASIC
Prenatal screening
G-NIPT® Lite
Core non-invasive prenatal screening for trisomy 21, 18, and 13, sex chromosome aneuploidies, and fetal sex confirmation.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- Streck cfDNA tube
- TAT
- ~17 days incl. shipping
Prenatal screening
G-NIPT® Premium
Expanded NIPT screening covering all autosomes, sex chromosome aneuploidies, fetal sex, selected CNVs, and CNVs larger than 7 Mb.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- Streck cfDNA tube
- TAT
- ~17 days incl. shipping
Prenatal screening
i-screen®
Non-invasive prenatal screening option performed from maternal EDTA whole blood.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- EDTA whole blood
- TAT
- ~17 days incl. shipping
Prenatal screening
NICE® Premium + Pathogen
Expanded NIPT screening with all autosomes, sex chromosome aneuploidies, 143 microdeletions, fetal sex, and a focused pathogen panel.
- Lab
- EDGC
- Method
- NGS
- Specimen
- Streck cfDNA tube
- TAT
- ~17 days incl. shipping
4 tests
Precision Oncology — Solid Tumor
Tumor profiling, HRD, and liquid biopsy pathways for solid cancers.
View clinical information →Tumor profiling
Tumor profiling
Solid Tumor — FFPE / Biopsy (+RNA)
Broad solid tumor profiling including hotspot mutations, full-exon coverage, CNV, RNA fusion analysis, MSI, and TMB.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- FFPE tissue
- TAT
- ~26 days incl. shipping
Tumor profiling
Solid Tumor — FFPE / Biopsy (excl. RNA)
DNA-focused solid tumor profiling from FFPE tissue when RNA analysis is not required or not feasible.
- Lab
- GC Genome
- Specimen
- FFPE tissue
- TAT
- ~19 days incl. shipping
Tumor profiling
GreenPlan® HRD
Homologous recombination deficiency testing from tumor tissue.
- Lab
- GC Genome
- Specimen
- FFPE tissue
Tumor profiling
Solid Tumor Liquid Biopsy (cfDNA)
Plasma cell-free DNA profiling covering SNV/indel, CNV, RNA fusion, TMB, and MSI where tissue is unavailable or insufficient.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- 2 × 10 mL Streck cfDNA tube
- TAT
- ~19 days incl. shipping
5 tests
Hematologic Oncology
NGS panels for acute leukemia, lymphoma, MDS/MPN, and plasma-cell neoplasms.
View clinical information →Hematologic malignancy
Hematologic malignancy
ALL Panel
Molecular profiling panel for acute lymphoblastic leukemia.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- EDTA whole blood / bone marrow
- TAT
- ~19 days incl. shipping
Hematologic malignancy
AML Panel
Molecular profiling panel for acute myeloid leukemia and related clinical questions.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- EDTA whole blood / bone marrow
- TAT
- ~19 days incl. shipping
Hematologic malignancy
Lymphoma Panel
A 60-gene panel for molecular characterization of lymphoid malignancies.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- EDTA whole blood / bone marrow
- TAT
- ~19 days incl. shipping
Hematologic malignancy
MDS / MPN Panel
Molecular profiling for myelodysplastic and myeloproliferative neoplasms.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- EDTA whole blood / bone marrow
- TAT
- ~19 days incl. shipping
Hematologic malignancy
Multiple Myeloma Panel
Molecular testing panel for plasma-cell neoplasms.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- EDTA whole blood / bone marrow
- TAT
- ~19 days incl. shipping
2 tests
Hereditary Cancer
Germline cancer predisposition testing and family-risk assessment.
View clinical information →Hereditary cancer
Hereditary cancer
Hereditary Cancer Panel (98 genes)
A 98-gene germline panel covering inherited cancer predisposition across 23 cancer types.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- EDTA whole blood
- TAT
- ~26 days incl. shipping
Hereditary cancer
Hereditary Women's Cancer Panel
Focused hereditary cancer panel for breast, ovarian, and other women's cancer risk indications.
- Lab
- GC Genome
- Specimen
- EDTA whole blood
- TAT
- ~22 days incl. shipping
14 tests
Rare Disease Genomics
Exome, genome, and targeted testing for rare or undiagnosed disease.
View clinical information →Exome / genome sequencingTargeted rare diseaseClinical genetics
Exome / genome sequencing
DGS — Proband
Genome sequencing for a proband with suspected rare or undiagnosed genetic disease.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- EDTA whole blood
- TAT
- ~70 days incl. shipping
Exome / genome sequencing
DGS — Trio
Trio-based genome sequencing for rare disease evaluation.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- EDTA whole blood
- TAT
- ~70 days incl. shipping
Targeted rare disease
Family Test (Sanger)
Targeted familial variant testing using Sanger sequencing.
- Method
- Sanger
- Specimen
- EDTA whole blood / amniotic fluid
- TAT
- Confirm with AC before quoting
Targeted rare disease
Fragile-X Screening
FMR1 repeat-expansion screening for Fragile X syndrome indications.
- Method
- Fragment analysis
- Specimen
- EDTA whole blood
- TAT
- ~17 days incl. shipping
Targeted rare disease
SMA — SMN1/SMN2 del/dup (MLPA)
SMN1/SMN2 dosage analysis for spinal muscular atrophy.
- Method
- MLPA
- Specimen
- EDTA whole blood
- TAT
- ~35 days incl. shipping
Exome / genome sequencing
WES — Proband (3 Billion)
Whole exome sequencing for a proband with suspected rare genetic disease.
- Lab
- 3billion
- Method
- NGS
- Specimen
- EDTA whole blood
- TAT
- ~45 days incl. shipping
Exome / genome sequencing
WES — Proband (GC Genome)
Whole exome sequencing through GC Genome for proband-only evaluation.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- EDTA whole blood
- TAT
- ~35 days incl. shipping
Exome / genome sequencing
WES — Trio (GC Genome)
Trio whole exome sequencing through GC Genome.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- EDTA whole blood
- TAT
- ~35 days incl. shipping
Exome / genome sequencing
Whole Genome Sequencing (3 Billion)
Whole genome sequencing for broad rare disease assessment.
- Lab
- 3billion
- Method
- NGS
- Specimen
- EDTA whole blood
- TAT
- ~40 days incl. shipping
Clinical genetics
ExomeDx — Exome Sequencing
Exome sequencing with interpretation against GeneDx's rare-disease dataset. Available proband-only, duo, or trio (patient plus one or both biological parents), with trio generally improving yield and reducing uncertain results. Holds FDA Breakthrough Device designation.
- Lab
- GeneDx
- Method
- Whole exome sequencing — proband, duo, or trio
- Specimen
- EDTA whole blood or buccal swab
- TAT
- ~29 days incl. shipping
Clinical genetics
GenomeDx — Genome Sequencing
Genome sequencing covering coding and non-coding regions, used where exome has been uninformative or a structural or non-coding cause is suspected. Holds FDA Breakthrough Device designation.
- Lab
- GeneDx
- Method
- Whole genome sequencing — proband, duo, or trio
- Specimen
- EDTA whole blood or buccal swab
- TAT
- ~38 days incl. shipping
Clinical genetics
GenomeDx ultraRapid — Inpatient Genome Sequencing
Accelerated genome sequencing for critically ill infants and children in the NICU or PICU, where a molecular diagnosis may change management within the admission. Requires coordination before collection — do not order this pathway without confirming the timeline with AC first.
- Lab
- GeneDx
- Method
- Rapid or ultra-rapid whole genome sequencing — duo or trio
- Specimen
- EDTA whole blood
- TAT
- ~18 days incl. shipping
Clinical genetics
Targeted Variant Testing (Familial)
Tests a relative for a specific variant already identified in the family, or confirms a variant reported elsewhere. Requires the prior report identifying the variant.
- Lab
- GeneDx
- Method
- Targeted analysis of a previously identified variant
- Specimen
- EDTA whole blood or buccal swab
- TAT
- ~38 days incl. shipping
Clinical genetics
ExomeDx, duo
Clinical exome sequencing of the patient and one biological parent for suspected monogenic disease.
- Lab
- GeneDx
- Method
- NGS
- TAT
- ~29 days incl. shipping
6 tests
Reproductive & Chromosomal
Chromosomal microarray and reproductive genetic testing pathways.
View clinical information →Chromosomal analysisClinical genetics
Chromosomal analysis
Chromosomal Microarray — EDGC (CMA)
Chromosomal microarray for developmental delay, autism spectrum disorder, congenital anomalies, and related indications.
- Lab
- EDGC
- Method
- SNP microarray
- Specimen
- EDTA blood / gDNA / amniotic fluid
- TAT
- ~23 days incl. shipping
Chromosomal analysis
Pregnancy Loss (All Chromosome, NGS)
All-chromosome deletion/duplication analysis for products of conception and pregnancy loss evaluation. Confirm specimen type and collection requirements with the reference laboratory before sampling.
- Lab
- EDGC
- Method
- NGS
- Specimen
- Sample requirements vary by test and reference laboratory
- TAT
- ~17 days incl. shipping
Clinical genetics
Prenatal Exome Sequencing
Exome sequencing for a fetus with structural anomalies on ultrasound where karyotype and microarray have been uninformative. Interpreted against GeneDx's prenatal exome dataset. Requires pre-test counselling and coordination — confirm specimen route and timeline with AC before the procedure.
- Lab
- GeneDx
- Method
- Whole exome sequencing on a prenatal specimen — trio preferred
- Specimen
- Amniotic fluid or CVS, with parental blood samples for trio analysis
- TAT
- ~29 days incl. shipping
Chromosomal analysis
Bebegene Basic
SNP array screening for 200–300 chromosomal abnormalities associated with rare disease.
- Lab
- EDGC
- Method
- SNP microarray
- Specimen
- EDTA whole blood
- TAT
- ~19 days incl. shipping
Chromosomal analysis
Bebegene Plus
Bebegene Basic coverage with an extended panel of microdeletion and microduplication regions.
- Lab
- EDGC
- Method
- SNP microarray
- Specimen
- EDTA whole blood
- TAT
- ~19 days incl. shipping
Chromosomal analysis
Bebegene Extended
The widest Bebegene configuration, covering around 1,001 microdeletion regions.
- Lab
- EDGC
- Method
- SNP microarray
- Specimen
- EDTA whole blood
- TAT
- ~19 days incl. shipping
7 tests
Preventive & Pharmacogenomics
Predictive health screening, pharmacogenetics, and disease-risk genomics.
View clinical information →Cancer early detectionPreventive genomicsPharmacogenetics
Cancer early detection
ai-CANCERCH®
Multi-cancer early detection from cfDNA; includes five cancer types for males and six cancer types for females, including ovarian cancer.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- Streck cfDNA tube
- TAT
- ~26 days incl. shipping
Preventive genomics
Genome Health (Female)
Polygenic risk assessment across 45 disease categories for females, including 14 cancer types.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- EDTA whole blood
- TAT
- ~19 days incl. shipping
Preventive genomics
Genome Health (Male)
Polygenic risk assessment across 44 disease categories for males, including neurological, cardiovascular, metabolic, and cancer risks.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- EDTA whole blood
- TAT
- ~19 days incl. shipping
Preventive genomics
Genome Screen — Cancer
Genomic screening focused on inherited cancer predisposition and risk stratification.
- Lab
- GC Genome
- Specimen
- EDTA whole blood
Preventive genomics
Genome Screen — Cardiac Arrest
A 40-gene screen covering 15 disease types, including hereditary arrhythmia syndromes.
- Lab
- GC Genome
- Method
- NGS
- Specimen
- EDTA whole blood
- TAT
- ~26 days incl. shipping
Pharmacogenetics
Pharmacogenetics (34 drugs)
Ten-gene pharmacogenetic panel predicting response across 34 drugs used in cardiometabolic, gastrointestinal, inflammatory, and other conditions.
- Lab
- GC Genome
- Method
- Real-time PCR
- Specimen
- EDTA whole blood
- TAT
- ~17 days incl. shipping
Preventive genomics
Telorisk®
Telomere-related risk assessment from peripheral blood.
- Lab
- GC Genome
- Specimen
- EDTA whole blood
- TAT
- ~15 days incl. shipping
6 tests
Consumer Wellness Genomics
Wellness-oriented genomic packages for lifestyle, predisposition, and personal insights.
Wellness genomicsClinical genetics
Wellness genomics
Gene2me (54 Wellness Options)
Wellness genomics covering healthcare, dietary, nutrition, fitness, beauty, ancestry, and other options.
- Lab
- EDGC
- Method
- SNP microarray
- Specimen
- EDTA whole blood
- TAT
- ~19 days incl. shipping
Wellness genomics
Gene2me Plus (18 Cancers + 11 Diseases)
SNP array covering selected cancer, common disease, and ophthalmic disease predisposition markers.
- Lab
- EDGC
- Method
- SNP microarray
- Specimen
- EDTA whole blood
- TAT
- ~19 days incl. shipping
Wellness genomics
GSA Package (Multi-panel Array)
Bundled multi-panel array package including Momcare, Gene2me Plus, MyEyeGene, Skincare, Ancestry, and more.
- Lab
- EDGC
- Method
- SNP microarray
- Specimen
- EDTA whole blood
- TAT
- ~19 days incl. shipping
Wellness genomics
KidsCare — Genetic Testing for Kids/Teens
Genetic predisposition screening across neuropsychological, dermatological, respiratory, refractive, nutritional, athletic, and chronic-condition markers.
- Lab
- EDGC
- Method
- SNP microarray
- Specimen
- EDTA whole blood
- TAT
- ~19 days incl. shipping
Wellness genomics
MyEyeGene (5 Ophthalmic Diseases)
Predisposition testing for macular degeneration, glaucoma, retinitis pigmentosa, keratoconus, and severe dry eye syndrome.
- Lab
- EDGC
- Method
- SNP microarray
- Specimen
- EDTA whole blood
- TAT
- ~19 days incl. shipping
Clinical genetics
Epi-Clock — Epigenetic Methylation Aging Analysis
DNA methylation analysis reporting biological age against chronological age.
- Lab
- EDGC
- Method
- MassArray
- Specimen
- EDTA whole blood
- TAT
- ~19 days incl. shipping
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