European ancestry associated_with SNVs

Subject: European ancestry
Relation: associated_with
Object: SNVs
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

The EA ... sample sizes provided ∼90% power to detect variants with a MAF ≥ 0.1%

confidence: 0.95