rare variation risk_factor_for disease susceptibility

Subject: rare variation
Relation: risk_factor_for
Object: disease susceptibility
p-value: —

Evidence from: primary | all sources

Evidence (1 sources)

Evolution and functional impact of rare coding variation from deep sequencing of human exomes. (2012) PMID:22604720 cited

rare variation likely makes an important contribution to ... disease susceptibility

confidence: 0.95