AA participants associated_with functional SNVs

Subject: AA participants
Relation: associated_with
Object: functional SNVs
p-value: 1e-15

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

AA individuals have a significantly higher proportion of predicted functional SNVs compared with EA individuals when the conservative definition is used (Wilcoxon-rank sum test; P < 10⁻15).

confidence: 0.95