Practise molecular assay selection, variant interpretation, cancer biomarkers, inherited disease testing and laboratory decisions for ABPath subspecialty preparation. These are independent learning materials, not official exam questions or a pass prediction.
Read the Molecular Genetic Pathology: Physician Subspecialty Preparation Guide study guide and official exam sourcesExam outline and official sources
American Board of Pathology (ABPath), in cooperation with the American Board of Medical Genetics and Genomics (ABMGG) · ABPath Molecular Genetic Pathology Exam Blueprint, explicitly updated for 2026; currently linked final Molecular Genetic Pathology Content Specifications, filename dated 2025-11-05; 2026 Booklet of Information, updated January 2026. The workbook label maps to this subspecialty certification examination. The assigned canonical slug is preserved. The content specifications do not state a separate effective date.
This original 20-question sample covers selected topics across the outline. It does not reproduce official exam questions or cover every tested topic.
- Molecular Genetic Pathology — ABPath
- 2026 ABPath Booklet of Information
- Subspecialty Exam Blueprints and Daily Exam Schedules — ABPath
- Molecular Genetic Pathology Exam Blueprint — Updated for 2026
- Content Specifications for Examinations — ABPath
- Molecular Genetic Pathology Content Specifications — Final
- General Management and Informatics Content Specifications — March 2026
- RNA Splicing — HGVS Nomenclature
- Glossary — HGVS Nomenclature
- Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test
- AMP/CAP Guidelines for Validation of Next-Generation Sequencing–Based Oncology Panels
- Good Laboratory Practices for Molecular Genetic Testing for Heritable Diseases and Conditions
- Laboratory Testing for KPC and NDM in Gram-negative Bacteria — CDC
- Genetic Testing FAQ — NHGRI
- Laboratory Testing for Fragile X, 2021 Revision — ACMG Technical Standard
- FMR1 Disorders — GeneReviews
- Spinal Muscular Atrophy — GeneReviews
- Pan-ethnic Carrier Screening and Prenatal Diagnosis for Spinal Muscular Atrophy
- Recurrence and Variability of Germline EPCAM Deletions in Lynch Syndrome
- BRCA Gene Changes: Cancer Risk and Genetic Testing — NCI
- ASCP/CAP/AMP/ASCO Colorectal Cancer Molecular Biomarkers — Summary of Recommendations
- The Landscape of MET Exon 14 Skipping Mutations in Patients With Lung Cancer
- 2025 European LeukemiaNet Recommendations for the Management of Chronic Myeloid Leukemia
- EuroClonality/BIOMED-2 Guidelines for Interpretation and Reporting of Ig/TCR Clonality Testing
- 2015 CPIC SSRI Guideline Supplement
- 2023 CPIC Guideline for Serotonin Reuptake Inhibitor Antidepressants
- SHEA/IDSA Clinical Practice Guideline for Clostridium difficile Infection
- Hematopoietic Chimerism Monitoring Based on STRs
- Naming Alleles — WHO HLA Nomenclature
- HTS Format Specifications — GA4GH/Samtools
- Variant Call Format Specification, Version 4.5
- 42 CFR 493.801 — Enrollment and Testing of Proficiency Testing Samples
- Technical standards and guidelines for spinal muscular atrophy testing | Genetics in Medicine
- s41431-019-0435-0.pdf
- s41431-022-01249-w.pdf
- clia-brochure-proficiency-testing-and-pt-referral-october-2024.pdf
- Numbering - HGVS Nomenclature
- s41436-021-01115-y.pdf
- 320196.pdf
- Standards_Guidelines_for_the_Interpretation_of_Sequence_Variants.pdf
Molecular Genetic Pathology Examination
Start with 20 free questions, then review the explanations and any topics you missed.
RNA testing demonstrates loss of exactly 84 coding nucleotides from a transcript, with no additional sequence change. What is the most accurate description of the downstream reading frame?
Molecular Genetic Pathology Examination
Flashcards
Normal Structure and Function
HGVS reference context
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