Skip to main content
. 2018;25(1):7–13. doi: 10.6001/actamedica.v25i1.3698

Table 2.

SNV statistics of 65 genome variants used in analysis

SNV Counts (%)
Intronic variants: 33 (53.23)
UTR 3’ variants 28 (84.84)
UTR 5’ variants 5 (15.16)
Exonic variants: 29 (46.77)
Synonymous 11 (37.93)
Nonsynonymous 17 (58.62)
Stopgain 1 (3.48)