Over 12,000 genetic variations that determine a person’s height have been found by researchers.
The 12,111 variations that cluster around areas of the genome involved with skeletal development provide a strong genetic predictor of height. The discovered variations account for 40% of the variance in height for persons of European ancestry and 10-20% for those of non-European ancestry.
Adult height is mostly determined by the information encoded in our DNA — children from tall parents tend to be taller and those from short parents are shorter, but these estimates aren’t perfect. Growth from a small baby into an adult, and the role genetics play in this, have traditionally been a complex and poorly understood area of human biology. Previously, the largest genome-wide association study looking at height used a sample size of up to 700,000 individuals, the current sample is about seven times more than previous studies.
The unprecedented scale of the research provides new levels of detail and biological insight as to why people are tall or short, with heritability being linked to various specific genomic regions. The findings show that genetic variants associated with height are concentrated in regions covering just over 20% of the genome.
The findings of the study might assist doctors discover patients who are unable to achieve their genetically projected height, which could then aid in the detection of hidden diseases or ailments that are stunting their growth or negatively influencing their health. The study also provides a significant model for how genome-wide investigations may be used to determine a disease’s biology and, ultimately, its genetic components.
While this study has a large number of participants from non-European ancestries compared to previous studies, the researchers emphasise the need for more diversity in genomic research.
Most of the genetic data available is from people of European ancestry, so genome-wide studies don’t capture the wide range of ancestral diversity across the globe. Increasing the size of genome-wide studies in non-European ancestry populations is essential to achieve the same level of saturation and close the gap in prediction accuracy in different populations.
Dr Eirini Marouli, co-first author of the study and Senior Lecturer in Computational Biology at Queen Mary University of London, said:
“We have accomplished a feat in studying the DNA of over 5 million people that was broadly considered impossible until recently.
“Genomic studies are revolutionary and might hold the key to solving many global health challenges — their potential is tremendously exciting. If we can get a clear picture of a trait such as height at a genomic level, we may then have the model to better diagnose and treat gene-influenced conditions like heart disease or schizophrenia, for example.
“If we can map specific parts of the genome to certain traits, it opens the door to widespread targeted, personalised treatments further down the line that could benefit people everywhere.”
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