candidate genes regulates SNVs
Evidence from:
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Evidence (1 sources)
Evolution and functional impact of rare coding variation from deep sequencing of human exomes.
(2012)
PMID:22604720
cited
gene length accounts for 76.6% of variation in the number of SNVs across genes (95% bootstrap CI = 73.9 to 79.1%; P < 10⁻15)
confidence: 0.94