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Texas Genetic Counselor Licensing Exam Practice Questions & Answers PDF 2026–2027

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Prepare with confidence using this Texas Genetic Counselor Licensing Exam Practice Questions & Answers PDF. Includes 100 multiple-choice practice questions, verified answers, detailed rationales, and comprehensive coverage of genetic counseling, medical genetics, inheritance patterns, prenatal testing, cancer genetics, ethics, and genomic medicine. Ideal for aspiring licensed genetic counselors, graduate students, and professionals seeking exam success. Instant digital download.

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Texas Genetic Counselor Licensing Exam –
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Practice Questions And Correct Answers (Verifi
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ed Answers) Plus Rationales 2026/2027 Q&A | In
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stant Download Pdf b b




1. Which of the following is the primary role of a genetic counselor?
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A. Perform gene-editing procedures b b


B. Provide nutritional counseling b b


C. Interpret genetic testing results and communicate risks
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D. Prescribe pharmacologic treatments b b


Genetic counselors specialize in interpreting genetic tests and conveying risks, option
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s, and implications to patients.
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2. The Genetic Information Nondiscrimination Act (GINA) protects individuals
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from:
A. All forms of genetic discrimination, including life insurance
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B. Discrimination in education settings b b b


C. Discrimination in health insurance and employment b b b b b


D. Discrimination in auto insurance premiums b b b b


GINA prohibits genetic discrimination in health insurance and employment, but n
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ot in life, disability, or long-term care insurance.
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3. Which of the following inheritance patterns is typical for cystic fibrosis?
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,A. X-linked recessive b


B. Autosomal recessive b


C. Autosomal dominant b


D. Mitochondrial
Cystic fibrosis follows an autosomal recessive inheritance, requiring two pathoge
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nic variants for disease expression.
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4. A patient with a BRCA1 mutation has which of the following increased risks?
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A. Colon cancer b


B. Breast and ovarian cancer b b b


C. Liver cancer b


D. Lung cancer b


BRCA1 mutations are associated primarily with elevated risks of breast and ovari
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an cancers.
b




5. Which ethical principle is emphasized when ensuring patients voluntarily
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consent to genetic testing?
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A. Beneficence
B. Justice
C. Autonomy
D. Non-maleficence
Autonomy ensures that patients make informed decisions without coercion.
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6. In pedigree analysis, a condition seen in every generation is most consistent
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with:
A. Autosomal dominant inheritance b b


B. Autosomal recessive inheritance b b


C. X-linked recessive inheritance b b

, D. Mitochondrial inheritance b


Autosomal dominant traits often appear in every generation.
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7. A heterozygous carrier couple for sickle cell disease has what probability of
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having an affected child?
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A. 0%
B. 25% unaffected, 75% affected
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C. 25% affected, 50% carrier, 25% unaffected
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D. 50% affected, 50% unaffected
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Mendelian ratios in autosomal recessive inheritance: 25% affected, 50% carriers, 25%
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unaffected.
b




8. Which test is most appropriate for diagnosing trisomy 21 in a newborn?
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A. Whole-genome sequencing b


B. Targeted mutation analysis b b


C. Karyotype analysis b


D. PCR
Karyotype analysis is the standard diagnostic method for identifying chromosom
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al aneuploidies such as trisomy 21.
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9. The ACMG guidelines classify variants into how many categories?
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A. Three
B. Four
C. Five (pathogenic, likely pathogenic, VUS, likely benign, benign)
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D. Six
The American College of Medical Genetics and Genomics uses five categories for vari
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ant interpretation.
b

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