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Principles of Inheritance and Variation is one of the most important chapters for Biology and regularly contributes questions in the NEET exam. Solving Principles of Inheritance and Variation NEET previous year questions (PYQs) helps students understand frequently tested concepts, improve problem-solving skills, and strengthen their command over genetics and heredity.
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Whether you are preparing for NEET 2027 or revising important Biology chapters, practising chapter-wise PYQs is an effective way to identify recurring question patterns and improve accuracy. This article provides year-wise NEET PYQs with detailed solutions, chapter analysis, preparation tips, common mistakes, and expert strategies. You can also refer to the latest RE-NEET 2026 Biology Question Paper for additional practice with recent exam-level questions.
The Principles of Inheritance and Variation chapter is one of the most important topics in NEET Biology, with questions consistently asked on Mendelian inheritance, chromosomal theory of inheritance, pedigree analysis, genetic disorders, linkage, and recombination. Solving NEET previous year questions (PYQs) helps candidates understand the latest question trends, improve conceptual clarity, and identify frequently tested topics. Along with previous year questions, aspirants can also practise the Principles of Inheritance and Variation RE-NEET 2026 questions to gain exposure to the latest exam-level questions and improve their preparation for NEET 2027.
NEET 2026
Q1. Given below are two statements: one is labelled as Assertion (A) and the other as Reason (R).
Assertion (A): In Mendel's monohybrid cross, all the F₁ plants were tall and none were dwarf.
Reason (R): Tallness is the dominant trait, while dwarfness is the recessive trait in pea plants.
Options:
Correct Answer: Option 2
Explanation: In Mendel's monohybrid cross, crossing pure tall (TT) with pure dwarf (tt) plants produced all tall (Tt) offspring in the F₁ generation because the tall allele is dominant over the dwarf allele.
Q 2. A person has blood group O. Which of the following parental genotype combinations cannot produce a child with blood group O?
Options:
Correct Answer: Option 1
Explanation: Blood group O has the genotype ii, so each parent must contribute an i allele. A father with genotype IᴬIᴮ does not carry the i allele, making it impossible for the child to inherit the ii genotype.
Q3. Given below are two statements:
Statement I: Down syndrome is caused by the absence of one X chromosome.
Statement II: Turner syndrome is caused by the presence of an extra chromosome.
Options:
Correct Answer: Option 3
Explanation: Down syndrome is caused by trisomy 21 (an extra copy of chromosome 21), whereas Turner syndrome results from monosomy X (45, X), where one X chromosome is absent. Therefore, both statements are incorrect.
NEET 2025
Q4. Genes R and Y follow independent assortment. If RRYY produces round yellow seeds and rryy produces wrinkled green seeds, what will be the phenotypic ratio of the F2 generation?
Difficulty Level: Medium
Option 1) Phenotypic ratio 9:7
Option 2) Phenotypic ratio 1:2:1
Option 3) Phenotypic ratio 3:1
Option 4) Phenotypic ratio 9:3:3:1
Solution:
Given -
The F1 generation will all be heterozygous RrYy and will display the dominant traits - round yellow seeds. Now,
The gametes for F2 from each parent will be: RY, Ry, rY, ry.
After fertilisation, the phenotypes:
Hence, the correct answer is option 4) Phenotypic ratio 9:3:3:1.
Q5. In a plant, the black seed colour (BB/Bb) is dominant over the white seed colour (bb). To find out the genotype of the black seed plant, which of the following genotypes will you cross?
NEET 2024
Difficulty level: Medium
Chapter: Principles of Inheritance and Variation
Option 1: BB
Option 2: bb
Option 3: Bb
Option 4: BB/Bb
Solution:
In a test cross, an organism with an unknown genotype is mated with an organism with a known genotype to ascertain the genotype of the unknown organism. The test cross is said to have been created by Gregor Mendel. To determine the genotype of a black seed colour at F2, the black seed from F2 is crossed with the white seed colour. This is called a test cross. To determine the genotype of the black seed (BB/Bb), we need to cross them with the white seed (bb)
Hence, the correct answer is Option (2) b
Q6. Broad palm with single palm crease is visible in a person suffering from –
NEET 2023
Difficulty level: Medium
Chapter: Principles of Inheritance and Variation
Option 1: Down's syndrome
Option 2: Turner's syndrome
Option 3: Klinefelter's syndrome
Option 4: Thalassemia
Solution:
A broad palm with a single palm crease, also known as a simian crease or a single transverse palmar crease, is commonly seen in individuals with Down syndrome. Down syndrome is a genetic disorder caused by the presence of an extra copy of chromosome 21. This condition is characterized by various physical and intellectual disabilities, and certain physical features are often associated with it.
One of the common physical features observed in individuals with Down syndrome is a single transverse palmar crease, where the normal two creases in the palm fuse into one. This can give the appearance of a broad palm with a single crease extending across the palm.
Therefore, the correct answer is Option (1) Down syndrome.
Q7. Which of the following occurs due to the presence of an autosome-linked dominant trait?
NEET 2022
Difficulty level: Easy
Chapter: Principles of Inheritance and Variation
Option 1: Myotonic Dystrophy
Option 2: Haemophilia
Option 3: Thalassemia
Option 4: Sickle cell anaemia
Solution:
Hemophilia is a disorder in which blood doesn’t clot normally, and it is an X-linked recessive disorder.
Thalassemia is a blood disorder involving a lower-than-normal amount of an oxygen-carrying protein. It is an autosomal recessive disorder.
Sickle cell anaemia is a group of disorders that causes red blood cells to become misshapen and break down. It is an autosomal recessive disorder.
Myotonic dystrophy is an autosomal dominant disorder,i.e., it occurs due to the presence of an autosomal-linked dominant trail.
Hence, the correct answer is option 1) Myotonic dystrophy.
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Marks Contribution: Approximately 8-12 marks in the NEET Biology paper.
Number of Questions: Typically 2-3 questions per exam, with some questions integrating diagram-based or pedigree-oriented questions.
| Year | Total Questions | Easy | Medium | Difficult |
|---|---|---|---|---|
| 2021 | 2 | 0 | 2 | 0 |
| 2022 | 5 | 0 | 5 | 0 |
| 2023 | 6 | 0 | 6 | 0 |
| 2024 | 4 | 0 | 4 | 0 |
| 2025 | 2 | 0 | 1 | 1 |
| 2026 | 3 | 1 | 2 | 0 |
Every year, 2-3 questions are consistently asked from Principles of Inheritance and Variation. The diagram-based questions are common as well. The most important topics that NEET 2027 students can prepare are given below in a table:
|
Subtopic |
Key Focus Areas | |
|---|---|---|
|
Mendelian Inheritance |
- Dihybrid and monohybrid crosses - Test cross and back cross - Ratio-based numerical problems | |
|
Deviation from Mendelian Ratios |
- Flower color in snapdragons (incomplete dominance) - Blood group inheritance (multiple alleles & codominance) - Lethal gene effects (e.g., coat colour in mice) | |
|
Gene Interaction |
- Coat color in Labrador dogs (epistasis) - Kernel colour in maize (complementary genes) - Human height and skin colour (polygenic inheritance) | |
|
Sex Determination |
- XO, XY, ZW, and haplodiploid systems - Drosophila sex determination - Barr body concept | |
|
Genetic Disorders |
- Sickle cell anaemia, Thalassemia (autosomal disorders) - Hemophilia, Color blindness (X-linked disorders) - Interpretation of pedigree charts | |
|
Linkage and Recombination |
- Difference between linkage and independent assortment - Calculation of recombination frequency - Chromosome mapping | |
|
Mutations |
- Point mutations (sickle cell anemia) - Frame-shift mutations - Mutagens and their effects | |
|
Human Genome Project & DNA Fingerprinting |
- Importance of HGP in medical genetics - Use of DNA fingerprinting in forensic science |
Below are ten important points for preparing Principles of Inheritance and Variation NEET questions:
Pay attention to learning Mendel's laws, genetic disorders, and patterns of inheritance to solve Principles of Inheritance and Variation NEET questions.
Practice Principles of Inheritance and Variation NEET questions from last year's papers to get used to the pattern and difficulty of the exam.
Practice Principles of Inheritance and Variation NEET previous year question paper consistently to build confidence and lower exam anxiety.
Identify and concentrate on commonly asked subjects in Principles of Inheritance and Variation NEET questions, including linkage and gene expression.
Practice a range of Principles of Inheritance and Variation NEET questions to enhance problem-solving and time-management skills.
Refer to NCERT notes as a basis for learning, as they include key concepts examined in Principles of Inheritance and Variation NEET pyq.
Use online platforms such as Careers360 for explanations and practice Principles of Inheritance and Variation NEET questions.
Compare your performance on Principles of Inheritance and Variation NEET questions to determine weak points and work on enhancing them.
Practice solving principles of inheritance and variation NEET pyq in a timed manner to optimize speed during the exam.
Practice principles of inheritance and variation NEET previous year question paper for rapid revision to ensure that you have mastered all major concepts before the exam.
Some common mistakes students make while preparing for NEET 2026 Principles of Inheritance and Variation questions:
Confusion in Mendelian Ratios
Students often mix up Mendelian ratios like 3:1, 9:3:3:1, and 1:2:1, leading to errors in solving inheritance problems. Misinterpreting test cross and back cross is another common mistake. Understanding the concept behind these ratios rather than just memorizing them can help in answering questions accurately.
Ignoring Non-Mendelian Inheritance
Many students focus only on Mendel’s laws and ignore topics like incomplete dominance, codominance, multiple alleles, and epistasis. However, NEET frequently asks about exceptions to Mendelian inheritance, especially blood group inheritance and coat colour genetics in animals.
Errors in Linkage and Recombination
Candidates often misinterpret Morgan’s experiment on linkage and recombination. Confusing crossing over with independent assortment and failing to calculate recombination frequency correctly can lead to wrong answers. Practising chromosome maps and numerical problems is essential to avoid these errors.
Difficulty in Pedigree Analysis
Many students struggle with interpreting pedigree charts, especially in identifying autosomal vs. sex-linked disorders. Misreading dominant and recessive traits can result in incorrect answers. A structured approach using flowcharts and practice questions can help in mastering pedigree analysis effectively.
Frequently Asked Questions (FAQs)
In NEET Biology, inheritance is the process by which traits and characteristics are passed from parents to offspring through genes.
The important topics in Principles of Inheritance and Variation Class 12 are Mendel’s laws, dihybrid and monohybrid crosses, test cross, blood group inheritance, sex determination, and genetic disorders.
Mendel's three laws are the Law of Dominance, Law of Segregation, and Law of Independent Assortment.
On Question asked by student community
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If NBE opens a correction
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