European ancestry associated_with SNV
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
AAs had significantly more SNVs per exome than EAs (15,073 versus 12,406, Mann-Whitney test, P < 10−16)
confidence: 0.99