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Consanguinity

Property of being from the same kinship as another person

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Consanguinity (from Latin cōnsanguinitās 'blood relationship, kinship') is the characteristic of having a kinship with a relative who is descended from a common ancestor.

Many jurisdictions have laws prohibiting people who are closely related by blood from marrying or having sexual relations with each other. The degree of consanguinity that gives rise to this prohibition varies from place to place. On the other hand, around 20% of the global population lives in areas where some consanguinous marriages are preferred. The degree of relationships are also used to determine heirs of an estate according to statutes that govern intestate succession, which also vary from jurisdiction to jurisdiction. In some communities and time periods, cousin marriage is allowed or even encouraged; in others, it is taboo, and considered to be incest.

The degree of relative consanguinity can be illustrated with a consanguinity table in which each level of lineal consanguinity (generation or meiosis) appears as a row, and individuals with a collaterally consanguineous relationship share the same row. The Knot System is a numerical notation that describes consanguinity using the Ahnentafel numbers of shared ancestors.

02Genetic definitions

Average DNA shared between relatives
Relationship Average DNA
shared %
self100%
parent / child50%
sibling50%
half-sibling25%
grandparent / grandchild25%
aunt / uncle / niece / nephew25%
half-aunt / half-uncle / half-niece / half-nephew12.5%
first cousin12.5%
half-first cousin6.25%
double-first cousin25%
great-grandparent / great-grandchild12.5%
grandaunt / granduncle / grandniece / grandnephew12.5%
first cousin once removed6.25%
second cousin3.125%

Genetically, consanguinity derives from the reduction in variation due to meiosis that occurs because of the smaller number of near ancestors. Because all humans share between 99.6% and 99.9% of their genome, consanguinity only affects a very small part of the sequence. If two siblings have a child, the child has only two rather than four grandparents. In these circumstances, the probability is increased that the child will inherit two copies of a harmful recessive gene (allele) (rather than only one, which is less likely to have harmful effects).

Genetic consanguinity is expressed as defined in 1922 by Wright with the coefficient of relationship r, where r is defined as the fraction of homozygous due to the consanguinity under discussion. Thus, a parent and child pair has a value of r=0.5 (sharing 50% of DNA), siblings have a value of r=0.5, a parent's sibling has r=0.25 (25% of DNA), and first cousins have r=0.125 (12.5% of DNA). These are often expressed in terms of a percentage of shared DNA but can be also popularly referred to as % of genes although that terminology is technically incorrect.

As a working definition, unions contracted between persons biologically related as second cousins or closer (r ≥ 0.03125) are categorized as consanguineous. This arbitrary limit has been chosen because the genetic influence in marriages between couples related to a lesser degree would usually be expected to differ only slightly from that observed in the general population. Globally it is estimated that at least 8.5% of children have consanguineous parents.

In clinical genetics, consanguinity is defined as a union between two individuals who are related as second cousins or closer, with the inbreeding coefficient (F) equal or higher than 0.0156, where (F) represents the proportion of genetic loci at which the child of a consanguineous couple might inherit identical gene copies from both parents.

A simplistic depiction of genetic relatedness after n generations as a 2−n progression
A simplistic depiction of genetic relatedness after n generations as a 2−n progression

03Epidemiology, rates of occurrence

Cultural factors in favor

Reasons favoring consanguinous marriage have been listed as higher compatibility between husband and wife sharing same social relationships, couples stability, enforcing family solidarity, easier financial negotiations and others. Consanguinity is a deeply rooted phenomenon in 20% of the world population, mostly in the Middle East, West Asia and North Africa. Globally, the most common form of consanguineous union is between first cousins, in which the spouses share 18 of their genes inherited from a common ancestor, and so their progeny are homozygous (or more correctly autozygous) at 116 of all loci (r = 0.0625). Due to variation in geographical and ethnic background and the loci chosen to genotype there is some 2.4% variation expected.

Europe

Historically, some European nobles cited a close degree of consanguinity when they required convenient grounds for divorce, especially in contexts where religious doctrine forbade the voluntary dissolution of a merely unhappy or childless marriage.

Muslim countries

In the Arab world, the practice of marrying relatives is common. According to the Centre for Arabic Genomic Research, between 40% and 54% of UAE nationals' marriages are between family members, up from 39% in the previous generation. Between 21% and 28% of marriages of UAE nationals were between first cousins. Consanguineous marriage is much less prevalent in Christian Arabs as they do not practice arranged marriages. Additionally, an indult dispensation is required to marriages contracted between first cousins or closer in Arab Christian denominations in communion with the Roman Catholic Church, and the Greek Orthodox Church; there are no similar regulations that apply to first-cousin marriages in the Coptic Orthodox Church.

In Egypt, around 40% of the population marry a cousin. A 1992 survey in Jordan found that 32% were married to a first cousin; a further 17.3% were married to more distant relatives. 67% of marriages in Saudi Arabia are between close relatives as are 54% of all marriages in Kuwait, whereas 18% of all Lebanese were between blood relatives. The incidence of consanguinity was 54.3% among Kuwaiti natives and higher among Bedouins.

It has been estimated that 55% of marriages between Pakistani Muslim immigrants in the United Kingdom are between first cousins, where preferential patrilateral parallel cousin marriage, i.e. a man marrying the daughter of his father's brother, is favored.

Double first cousins are descended from two pairs of siblings, and have the same genetic similarity as half-siblings. In unions between double first cousins, the highest inbreeding coefficients are reached, with an (F) of 0.125, for example among Arabs and uncle-niece marriages in South India.

Quebec

The early days of colonization, particularly from 1660 to 1680, gave French Canadians genetic traits that are still present today, owing to the isolation and low population of the early colony. This has led to the province having a higher rate of hypercholesterolemia, tyrosinemia, spastic ataxia, intestinal atresia, myotonic dystrophy, etc., in the population than anywhere else in the world.

Diagram of common family relationships, where the area of each colored circle is scaled according to the coefficient of relatedness. All relatives of the same relatedness are included together in one of the gray ellipses. Legal degrees of relationship can be found by counting the number of solid-line connections between the self and a relative.
Diagram of common family relationships, where the area of each colored circle is scaled according to the coefficient of relatedness. All relatives of the same relatedness are included together in one of the gray ellipses. Legal degrees of relationship can be found by counting the number of solid-line connections between the self and a relative.

04Genetic disorders

The phenomenon of inbreeding increases the level of homozygotes for autosomal genetic disorders and generally leads to a decreased biological fitness of a population known as inbreeding depression, a major objective in clinical studies. While the risks of inbreeding are well-known, informing minority group families with a tradition of endogamy and changing their behavior is a challenging task for genetic counseling in the health care system. The offspring of consanguineous relationships are at greater risk of certain genetic disorders. Autosomal recessive disorders occur in individuals who are homozygous for a particular recessive gene mutation. This means that they carry two copies (alleles) of the same gene. Except in certain rare circumstances (new mutations or uniparental disomy) both parents of an individual with such a disorder will be carriers of the gene. Such carriers are not affected and will not display any signs that they are carriers, and so may be unaware that they carry the mutated gene. As relatives share a proportion of their genes, it is much more likely that related parents will be carriers of an autosomal recessive gene, and therefore their children are at a higher risk of an autosomal recessive disorder. The extent to which the risk increases depends on the degree of genetic relationship between the parents; so the risk is greater in mating relationships where the parents are close relatives, but for relationships between more distant relatives, such as second cousins, the risk is lower (although still greater than the general population).

Consanguinity in a population increases its susceptibility to many infectious pathogens such as tuberculosis and hepatitis, but may decrease its susceptibility to malaria and some other pathogens.

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Sources and credits

This article is adapted from the Wikipedia article Consanguinity, written by its contributors and licensed under CC BY-SA 4.0. Fathomly has changed the layout, removed citation markers, navigation and maintenance notices, and adjusted punctuation. This adapted version is shared under the same license. For references, see the original article.

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