singletons associated_with SNV

Subject: singletons
Relation: associated_with
Object: SNV
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

Of the total SNVs, 57% (285,857) were singletons.

confidence: 0.95