A positively selected, common, missense variant in FBN1 confers a 2.2 centimeter reduction of height in the Peruvian population
Samira AsgariiD, Yang LuoiD, Gillian M. BelbiniD, Eric BartelliD, Roger I. CalderoniD, Kamil SlowikowskiiD, Carmen C. ContrerasiD, Rosa M. YatacoiD, Jerome Timothy GaleaiD, Judith JiméneziD, Julia M. CoitiD, Chandel Farroñay-GarcíaiD, Rosalynn M. NazarianiD, Timothy D. O’ConnoriD, Harry C. DietziD, Joel N. HirschhorniD, Heinner GuioiD, Leonid W. LeccaiD, Eimear E. KennyiD, Esther Ellen FreemaniD, Megan B. MurrayiD, Soumya RaychaudhuriiD
Abstract
Peruvians are among the shortest people in the world. To understand the genetic basis of short stature in Peru, we examined an ethnically diverse group of Peruvians and identified a novel, population-specific, missense variant in FBN1 (E1297G) that is significantly associated with lower height in the Peruvian population. Each copy of the minor allele (frequency = 4.7%) reduces height by 2.2 cm (4.4 cm in homozygous individuals). This is the largest effect size known for a common height-associated variant. This variant shows strong evidence of positive selection within the Peruvian population and is significantly more frequent in Native American populations from coastal regions of Peru compared to populations from the Andes or the Amazon, suggesting that short stature in Peruvians is the result of adaptation to the coastal environment. One Sentence SummaryA mutation found in Peruvians has the largest known effect on height for a common variant. This variant is specific to Native American ancestry.
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