Genetics of blood type: Inheritance and compatibility

Medicover Genetics Editorial Team|

Scientifically checkedView our editorial guidelines
Scientifically checked

About 118.54 million blood donations are collected worldwide [, WHO]. Knowing your blood type is important for medical reasons, e.g. if you require a blood transfusion or if you want to donate blood []. Blood typing is a fast and easy way to ensure that you receive the right blood type during surgery or after an injury. Incompatible blood can trigger a dangerous immune response. Blood typing is also important for pregnant women to prevent Rhesus incompatibility between mom and baby.

ABO blood types

The blood type is determined by the antigen on the surface of the red blood cells []. There are four main blood groups (A, B, AB, or O) and a Rhesus (Rh) factor (positive or negative). The blood type is passed down from our parents. The A and B alleles are co-dominant and the O allele is recessive [].

Molecular basis

The ABO gene is located on chromosome 9 and has three alleles, A, B and O []. The A allele encodes a glycosyltransferase that adds N-acetylgalactosamine to the glycoprotein H antigen that is expressed on all normal red cells. The B allele encodes a different glycosyltransferase that adds d-galactose. The O allele is a deletion that results in loss of enzyme translation (inactive glycosyltransferase); therefore, resulting in an unmodified H antigen. A and B are co-dominant alleles, as a result, AB individuals express both antigens.

Possible blood types

Those are the six possible ways these alleles can be combined resulting in one of the four blood types []:

Genotype
Blood type
AAA
AOA
BBB
BOB
ABAB
OOO

Depending on the parent alleles, those are all possible combinations for the baby []:

Parent alleles
AA
BB
AB
OO
AO
BO
AAAAABAA, ABAOAA, AOAB, AO
BBABBBAB, BBBOAB, BOBB, BO
ABAA, ABAB,BBAA, BB, ABAO,BOAA, AO, BO, ABBB, AO, AB, AO
OOAOBOAO, BOOOAO, OOBO, OO
AOAA, AOAB, BOAA, AB, AO, BOAA,OOAA, AO, OOAO, BO, AB, OO
BOAO, ABBB, BOAB, AO, BB, BOBO,OOAB, AO, BO, OOBB, BO, OO

Blood type compatibility

The ABO blood type is based on the presence or absence of the A and B antigens on the red blood cells. People with the A blood type have only the A antigen, while people with the B blood type have only the B antigen. AB blood type has both A and B antigens, and O blood type has neither A nor B antigens.

By six months old, you have developed immunity against the antigens your red blood cells lack. People with the A blood type have antibodies against the B blood type, and people with the B blood type have antibodies against the A blood type. If you have type A blood, you cannot get type B blood because your body’s anti-B antibodies fight the B antigens in B blood.

AB positive blood (AB+) is considered the universal recipient, and O negative blood (O-) is considered the universal donor.

Blood type compatability
O-
O+
B-
B+
A-
A+
AB+
O-✓------
O+✓✓-----
B-✓-✓----
B+✓✓✓✓---
A-✓---✓--
A+✓✓--✓✓-
AB-✓-✓-✓-✓
AB+✓✓✓✓✓✓✓

Table from [].

ABO blood group and associated health risk

The ABO blood group system has been linked to several diseases, primarily cardiovascular problems []. The determination of ABO blood groups could serve in blood group individualised approaches towards health maintenance and prevention of diseases.

A study from 2020 published in Arteriosclerosis, Thrombosis, and Vascular Biology (AHA journals) showed that ABO blood groups were associated with 11 health and disease outcomes. ABO blood groups were primarily associated with cardiovascular outcomes. Individuals with blood group A and B were associated with hyperlipidemia, thrombosis, myocardial infarction and heart failure. Whereas, individuals with O blood groups were associated with hypertension.

Rhesus factor

The  is a protein that is found on the surface of red blood cells. If your red blood cells contain this protein, you are Rh positive. If your blood cells do not have this protein, you are Rh negative. Everyone inherits one Rh factor gene from each parent.

Depending on the parent’s Rh factor, the child could have the following Rh factor:

Parent Rh factor
Rh-/Rh-
Rh+/Rh+
Rh-/Rh+
Rh-/Rh-Rh-Rh+Rh-, Rh+
(Rh-/Rh+)
Rh+/Rh+Rh+Rh+Rh+, Rh+
(Rh-/Rh+)
Rh-/Rh+Rh-, Rh+
(Rh-/Rh+)
Rh+, Rh+Rh-, Rh+, Rh+
(Rh-/Rh+)

Table from []
Keep the following in mind:
Rh-/Rh- = Rh- factor
Rh-/Rh+ = Rh+ factor
Rh+/Rh+ = Rh+ factor

Rhesus factor compatibility

A medical problem can occur when a woman, who is Rh-, is pregnant with a Rh+ foetus []. The first child may have no difficulty, but subsequent similar pregnancies may produce severely anaemic newborns. Exposure to the red blood cells of the first Rh+ foetus appears to protect the Rh- mother, thus potentially preventing her from developing antibodies that can cause brain damage in any subsequent Rh+ foetus. Damage to the fetal brain can occur as a result of the severe destruction of red blood cells. There are preventable measures available to prevent the severe effects of Rh incompatibility by transfusions to the foetus within the uterus. However, genetic counselling before conception is helpful so that the mother can receive Rh immunoglobulin immediately after her first and any subsequent pregnancies involving a Rh+ foetus.

This immunoglobulin effectively destroys the fetal red blood cells before the mother’s immune system is stimulated. Therefore, the mother avoids becoming actively immunised against the Rh antigen and will not produce antibodies that could attack the red blood cells of a future Rh+ foetus.

Last updated: 17.06.2026

Latest articles

All about genetics
Health and well-being
Hereditary diseases
  • VERACITY

    New-generation non-invasive prenatal screening from week 9 of pregnancy, analysing fetal cell-free DNA in maternal blood to detect selected chromosomal abnormalities with high sensitivity and specificity for early and reliable prenatal risk assessment.

  • Pharmacogenomics

    Enabling personalised treatments for safer, more effective care through genetic insights that guide optimal prescribing from the start and refine therapy when patients experience side effects or poor response.

  • ebiom+

    A comprehensive assessment of the endometrial microbiome and chronic endometritis pathogens to enhance clinical outcomes, prevent treatment delays, and support a more informed, personalised fertility care.

  • WES

    Advanced sequencing that simultaneously analyses a broad range of genes to detect the genetic basis of complex diseases, improve diagnostic accuracy, and inform recurrence risk assessment for better clinical decision-making.

Why Medicover Genetics

Leader in genetic testing with >25 years of experience in counselling and diagnostics

Comprehensive CE-IVD kit portfolio and seamless Technology Transfer solution for laboratories of any size

End-to-end clinical workflow from sample processing to sequencing analysis and reporting

CAP- and CLIA- and ISO15189 accredited, GMP- and ISO9001 and 13485 certified

Are you a patient?

Are you a physician?