PolyFun targets SNP

Subject: PolyFun
Relation: targets
Object: SNP
p-value: —

Evidence from: primary | all sources

Evidence (2 sources)

Functionally informed fine-mapping and polygenic localization of complex trait heritability. (2020) PMID:33199916 cited

PolyFun software will primarily be used to fine-map genome-wide significant loci, which harbor most PIP>0.95 SNPs.

confidence: 0.96

Functionally informed fine-mapping and polygenic localization of complex trait heritability. (2020) PMID:33199916 cited

setting prior causal probabilities for SNPs on the target chromosome

confidence: 0.92