Blood type of a child with type B and type O parents
Can type B and type O parents have a type O child?
Yes, if the type B parent is BO. A BO parent passes on O half the time and a type O parent always does, so with the genotype unknown the chance of a type O child is 47.4% with US figures and 47.6% with England’s. The child is type B or O, never A or AB by ordinary inheritance.
Chance of each blood type
| Child’s type | US | England |
|---|---|---|
| Type A | not possible | not possible |
| Type B | 52.6% | 52.4% |
| Type AB | not possible | not possible |
| Type O | 47.4% | 47.6% |
Genotype odds worked out from Stanford Blood Center’s estimates for the US population (“Blood Types”, read October 9, 2026; general estimates for teaching, taken from the AABB Technical Manual, 18th edition) and NHS Blood and Transplant’s shares of donors in England (“Blood types”, read October 9, 2026; accurate at February 2026 and rounded to whole numbers).
The values are facts and free to use; this page’s selection and presentation are © 2026 ScienceQuest.
Open type B and type O parents in the blood type calculator to add Rh, grandparents’ types or a genotype you already know.
Punnett squares for each genotype pairing
In each square the type B parent’s alleles run across the top and the type O parent’s down the side, and each box is one equally likely child.
| Alleles of parent 2 | B | B |
|---|---|---|
| O | BO type B | BO type B |
| O | BO type B | BO type B |
| Alleles of parent 2 | B | O |
|---|---|---|
| O | BO type B | OO type O |
| O | BO type B | OO type O |
A grandparent’s type can settle which square applies: a type B parent whose own mother or father is type O must be BO. Weighting every square by how likely its pairing is, and adding them up, gives the chances in the table above.
The weighted square
The calculator draws a single square instead, with each parent’s side split by how likely that parent is to pass on each allele, so a box’s chance is the product of its column and its row. The split comes from Hardy-Weinberg proportions. A type B person is BO 94.8% of the time on US figures and 95.1% on England’s. The Hardy-Weinberg calculator works through the same proportions for a gene with two alleles.
| Alleles of parent 2 | B 0.52598 | O 0.47402 |
|---|---|---|
| O 1 | BO type B 0.52598 | OO type O 0.47402 |
| Alleles of parent 2 | B 0.52441 | O 0.47559 |
|---|---|---|
| O 1 | BO type B 0.52441 | OO type O 0.47559 |
Chance of a type O child on US figures
- Shares from Stanford Blood Center’s estimates for the US population: A 42%, B 10%, AB 4%, O 44%, Rh negative 15%.
- r = √O = √0.44 = 0.66332, p = 1 − √(O + B) = 0.26515, q = 1 − √(O + A) = 0.072638
- D = 1 − p − q − r = −0.0011162, so p = 0.26501, q = 0.072598 and r = 1 − p − q = 0.6624
- Parent 1 is type B: P(BO | B) = 2qr / (q² + 2qr) = 0.096177 / 0.10145 = 0.94805, so it passes on B with 0.52598 and O with 0.47402.
- Parent 2 is type O, so OO: every gamete carries O.
- P(x, y) is the chance that parent 1 passes on x and parent 2 passes on y: the two chances multiplied.
- P(O) = P(O, O) = 0.47402 × 1 = 0.47402
- Check: the square has one O box, of area 0.47402.
Rh factor
Rh is inherited apart from ABO: RHD is on chromosome 1 and ABO on chromosome 9, so the chance of a type such as B+ is its ABO chance times its Rh chance. An Rh positive parent is DD or Dd, and is Dd 55.8% of the time on US figures, where 15% of people are Rh negative, and 67.5% on England’s, where 26% are.
| Child’s type | US | England |
|---|---|---|
| B+ | 48.5% | 46.5% |
| B− | 4.1% | 5.98% |
| O+ | 43.7% | 42.1% |
| O− | 3.69% | 5.42% |
With one Rh positive and one Rh negative parent, the chance of an Rh negative child is 27.9% on US figures and 33.8% on England’s. Two Rh negative parents have only Rh negative children by ordinary inheritance, although weak or partial D can type differently from one test to another. None of this replaces the blood tests of prenatal care.
Rare exceptions
Each of these can explain a child typed as A or AB, a type the squares above rule out.
The Bombay phenotype
A person with two non-working copies of the H gene (hh) cannot make the H antigen that A and B are built on, so tests as type O whatever ABO alleles they carry. If the type O parent is hh and carries A, a child who gets that A, and a working H gene from the type B parent, can test as type A or AB. It was first described in Bombay, now Mumbai, in 1952.
Weak A or B subgroups
Some A and B alleles make so little antigen that a routine test can miss it. So either parent may carry a weak A allele that their own test missed. A child who inherits it carries A too, and a test that picks up the weak antigen types the child as A or AB.
Chimerism, where one body has two cell lines such as blood cells from a twin, and a bone marrow transplant can each give a blood type that differs from the alleles a person passes on, and a mislabeled sample or a wrong record produces the same surprise. The genetic exceptions are rare. An unexpected type is a reason to recheck, not proof that someone is not a parent; parentage is settled by DNA testing.