SNVs associated_with European ancestry
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
median number of SNVs per gene ... significantly different ... between AAs (median of 16 ...) and EAs (median of 13 ...) (P < 10⁻15)
confidence: 0.96