EA participants associated_with functional SNVs
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
EA individuals have a significantly higher proportion of predicted functional SNVs compared with AA individuals (Wilcoxon-rank sum test; P < 10⁻15).
confidence: 0.95