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Unique roles of rare variants in the genetics of complex diseases in humans
Genome-wide association studies have identified >10,000 genetic variants associated with various phenotypes and diseases. Although the majority are common variants, rare variants with >0.1% of minor allele frequency have been investigated by imputation and using disease-specific custom SNP arr...
Guardat en:
| Publicat a: | J Hum Genet |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer Singapore
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7728599/ https://ncbi.nlm.nih.gov/pubmed/32948841 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s10038-020-00845-2 |
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