associated SNPs associated_with complex diseases
Evidence from:
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all sources
Evidence (2 sources)
resolve the heritability attributed to common variation to a finite set of SNPs (and small genomic regions). These variants ... would be most relevant to address questions of function, mechanism and therapeutic intervention.
confidence: 0.85
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.
(2017)
PMID:27663502
cited
genetic variation affecting complex phenotypes is tagged by SNPs on genome-wide arrays
confidence: 0.95