Middle Eastern Genetic Variation Improves Clinical Annotation of the Human Genome
Sathishkumar RamaswamyiD, Ruchi JainiD, Maha El Naofal, Nour Halabi, Sawsan Yaslam, Alan TayloriD, Ahmad N. Abou TayouniD
Abstract
Genetic variation in populations of Middle Eastern origin remains highly underrepresented in most comprehensive genomic databases. This underrepresentation hampers the functional annotation of the human genome and challenges accurate clinical variant interpretation. To highlight the importance of capturing genetic variation in the Middle East, we aggregated whole exome and genome sequencing data from 2116 individuals in the Middle East and established the Middle East Variation (MEV) database. Of the high-impact coding (missense and loss of function) variants in this database, 53% were absent from the most comprehensive Genome Aggregation Database (gnomAD), thus representing a unique Middle Eastern variation dataset which might directly impact clinical variant interpretation. We highlight 39 variants with minor allele frequency >1% in the MEV database that were previously reported as rare disease variants in ClinVar and the Human Gene Mutation Database (HGMD). Furthermore, the MEV database consisted of 281 putative homozygous loss of function (LoF) variants, or complete knockouts, of which 31.7% (89/281) were absent from gnomAD. This set represents either complete knockouts of 83 unique genes in reportedly healthy individuals, with implications regarding disease penetrance and expressivity, or might affect dispensable exons, thus refining the clinical annotation of those regions. Intriguingly, 24 of those genes have several clinically significant variants reported in ClinVar and/or HGMD. Our study shows that genetic variation in the Middle East improves functional annotation and clinical interpretation of the genome and emphasizes the need for expanding sequencing studies in the Middle East and other underrepresented populations.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 15
- FWCI
- 1.21
- Field percentile
- top 24%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- A Foundational Exome Resource for Jordan: Dual Ancestry Admixture and Population-Specific Variants to Improve Clinical Variant Interpretation
Tawfiq Jamal Froukh·medRxiv·May 27, 2026
- Most disease gene variants show minimal population differentiation despite incomplete coverage
Simon Gyimah·bioRxiv·Jan 5, 2026
- A deep catalog of protein-coding variation in 985,830 individuals
Kathie Sun, Xiaodong Bai, … Suganthi Balasubramanian·bioRxiv·May 9, 2023
- Expanding the Russian allele frequency reference via cross-laboratory data integration: insights from 7,452 exome samples
Yury A. Barbitoff, Хмелькова Дарья Николаевна, … Alexander V. Predeus·National Science ReviewPeer-reviewed·Sep 13, 2024
- Incomplete annotation of disease-associated genes is limiting our understanding of Mendelian and complex neurogenetic disorders
David Zhang, Sebastian Guelfi, … Mina Ryten·Science AdvancesPeer-reviewed·Jun 10, 2020
- Qatar Genome: Insights on Genomics from the Middle East
Hamdi Mbarek, Geethanjali Devadoss Gandhi, … Asma Al-Thani·Human MutationPeer-reviewed·Feb 2, 2022