MCTFR associated_with imputation accuracy
Evidence from:
primary |
all sources
Evidence (1 sources)
In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes.
(2014)
PMID:25387710
cited
imputation using the MCTFR sequences performed noticeably better, resulting in increases of .2–.3 in the dosage R2 value for SNPs with MAF < 1%
confidence: 0.95