Blood Type Inheritance Calculator

Calculate blood type compatibility, inheritance probabilities, and transfusion safety. Essential tool for genetics, medicine, and personal health awareness.

Father's Blood Type
Mother's Blood Type
? Both O+
? A+ & B+ (all types possible)
? AB+ & O- (interesting mix)
⚖️ Both Rh- → 100% Rh- child
? A+ & A+ → possible O child
Privacy first: All calculations happen locally. No data leaves your device.

How Blood Type Inheritance Works

The ABO blood group system is determined by a single gene with three alleles: A, B, and O. Each person inherits two copies (one from each parent). Alleles A and B are co-dominant, while O is recessive. The Rh system is governed by the RHD gene: Rh-positive (Rh+) is dominant over Rh-negative (Rh-). This calculator uses Mendelian genetics to enumerate all possible genotype combinations and compute precise offspring probabilities.

Scientific basis: The model assumes Hardy-Weinberg principles for genotype probability when the exact parental genotype is unknown (e.g., a person with type A may be AA or AO). Each possible parental genotype is weighted equally, reflecting standard genetic counseling practice. The final probabilities represent the total likelihood over all hidden genetic possibilities.

ABO Inheritance Patterns

Parent 1 Parent 2 Child Possible Blood Types Probability Range*
O O O 100%
O A A or O ~50% A, 50% O (if A parent is AO) or 100% A (if AA)
O B B or O Variable depending on B parent genotype
O AB A or B 50% A, 50% B
A A A or O Approx 75% A, 25% O if both AO
A B A, B, AB, O All four possible (25% each if both heterozygous)
A AB A, B, AB 50% A, 25% AB, 25% B
B B B or O 75% B, 25% O (both BO)
B AB A, B, AB 50% B, 25% A, 25% AB
AB AB A, B, AB 25% A, 50% AB, 25% B

* Probabilities depend on hidden parental genotypes; our calculator computes the exact aggregated probability across all possible genotype combinations.

Rh Incompatibility in Pregnancy

If an Rh- mother carries an Rh+ baby, her immune system may produce antibodies that attack red blood cells in a subsequent Rh+ pregnancy, leading to hemolytic disease of the newborn (HDN). This calculator estimates the probability of Rh+ offspring. Preventive treatment with Rho(D) immune globulin (RhoGAM) is highly effective. Early prenatal care is essential.

Global Frequency of Blood Types

Distribution varies by population. For example, O+ is the most common worldwide (~37%), followed by A+ (~27%). Rh-negative individuals are rarer, especially in Asia (e.g., <1% in China) but more common in Europe (~15%). These frequencies influence blood bank supply and transfusion planning.

United States: O+ 37%, A+ 36%, B+ 9%, AB+ 3%, Rh- total ~15%
Global average: O+ 37%, A+ 27%, B+ 22%, AB+ 6%, Rh- ~10%

Rare Blood Types and Variations

Bombay phenotype (hh): A rare recessive condition where individuals lack the H antigen, appearing as type O regardless of ABO genotype. They can only receive blood from other Bombay donors. Our calculator assumes standard ABO inheritance and does not account for such ultra-rare variants. Cis-AB and other chimeras exist but are extremely rare.

Historical & Scientific Context

Karl Landsteiner discovered the ABO system in 1901, earning the Nobel Prize. The Rh factor was identified in 1937 by Landsteiner and Wiener. Understanding these systems has saved millions of lives through safe transfusion and prenatal care.

Rh Factor Inheritance: Simple Dominance

The Rh protein is produced if at least one RHD allele is present (Rh+). Rh- individuals have two recessive alleles (dd). For a child to be Rh-, both parents must carry the recessive d allele. The calculator accounts for the fact that Rh+ parents may be either DD (homozygous) or Dd (heterozygous). This yields realistic probabilities, especially important for prenatal care (Rh incompatibility).

Clinical Relevance: Hemolytic Disease of the Newborn

Understanding Rh inheritance is critical for preventing hemolytic disease of the newborn (HDN). If an Rh- mother carries an Rh+ child, she may produce antibodies that affect subsequent pregnancies. This calculator highlights the probability of Rh+ offspring, empowering family planning and medical awareness. Always consult healthcare providers for Rh immunoglobulin prophylaxis when indicated.

Frequently Asked Questions

Yes! For example, two parents with type A (both genotype AO) can have a child with type O. Similarly, an A parent and a B parent can have a child with AB or O depending on alleles. The calculator reveals these non-intuitive outcomes.

The calculator provides mathematically accurate probabilities based on Mendelian inheritance. However, rare mutations (e.g., cis-AB, Bombay phenotype) are not considered. For paternity or medical diagnostics, lab tests remain the gold standard.

Because Rh+ individuals can be either homozygous (DD) or heterozygous (Dd). Our algorithm accounts for both possibilities with equal weight, delivering realistic aggregate probabilities. If both parents are Rh+, there is still a chance (around 6% if both are carriers) for an Rh- child.

Blood type alone cannot confirm paternity, but it can exclude a potential father if the child’s blood type is genetically impossible given the parents’ types. This tool helps identify such impossible scenarios. Always rely on DNA testing for legal or definitive purposes.

A rare recessive condition where individuals lack the H antigen, appearing as type O regardless of ABO genotype. This calculator assumes standard ABO inheritance without rare variants; for medical cases, genotyping is recommended.
References: NCBI – ABO Blood Group System, Dean L. “Blood Groups and Red Cell Antigens” (2005), AABB Clinical Guidelines, Genome.gov – Rh Factor.
Last evidence-based review: March 2025. All calculations follow standard genetic principles.

This tool reflects consensus from medical genetics resources, peer-reviewed inheritance models, and was validated by biology educators. Every computation incorporates both ABO and Rh systems with unbiased genotype weighting to give the most complete prediction for educational and planning purposes.Last reviewed March 2026