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A phenome-wide scan reveals convergence of common and rare variant associations
BACKGROUND: Common and rare variants contribute to the etiology of complex traits. However, the extent to which the phenotypic effects of common and rare variants involve shared molecular mediators remains poorly understood. The question is essential to the basic and translational goals of the scien...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683189/ https://www.ncbi.nlm.nih.gov/pubmed/38017547 http://dx.doi.org/10.1186/s13073-023-01253-9 |