From: Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects
Chromosome position
Variants
VSD and TOF cases (26)
Control (10)
17: 16068377-16068377
G207C
4/26 (15.35%)
Nil
17: 16068343-16068343
C241T
5/26 (19.2%)
17: 16068340-16068340
G244A
12/26 (46.1%)