SNVs associated_with candidate genes

Subject: SNVs
Relation: associated_with
Object: candidate genes
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

503,481 SNVs identified in 15,585 genes

confidence: 0.95