Sequencing of 19,219 exomes identifies a low-frequency variant inFKBP5promoter predisposing to high myopia in a Han Chinese population

SUMMARY High myopia (HM) is one of the leading causes of visual impairment and blindness worldwide. Here, we report a whole-exome sequencing (WES) study in 9,613 HM cases and 9,606 controls of Han Chinese ancestry to pinpoint HM-associated risk variants. Single-variant association analysis identified three novel genetic loci associated with HM, including an East Asian ancestry-specific low-frequency variant (rs533280354) in FKBP5 . Multi-ancestry meta-analysis with WES data of 2,696 HM cases and 7,186 controls of European ancestry from the UK Biobank discerned a novel European ancestry-specific rare variant in FOLH1 . Functional experiments revealed a mechanism whereby a single G to A transition at rs533280354 disrupted the binding of transcription activator KLF15 to the promoter of FKBP5 , resulting in decreased transcription of FKBP5 . Furthermore, burden tests showed a significant excess of rare protein-truncating variants among HM cases involved in retinal blood vessel morphogenesis and neurotransmitter transport.