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SNPs + GWAS - Coggle Diagram
SNPs + GWAS
GWAS
Defined as any study of genetic variation across the entire human genome that is designed to identify genetic associations w/ observable traits (BP/weight) or presence/absence of disease (cancer) or condition
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Large proportion of heritability remains unexplained by GWAS and very limited functional knowledge is known at most identified loci
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Disease
Very few diseases are monogenetic as most are multifactorial influenced by both genetics and environmental factors
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Human Genome
23 chromosome pairs, 3 billion bases