All of V2369

ID Consequence Gene/Location Detail Geno Type CHD Type
S4653 intron_variant DNMT1 NC_000019.10:g.10146569G>A G/G isolated CHD/non-isolated CHD: VSD/ASD/TOF/PDA/PAH/DORV/PS/AS/VSD, PFO/VSD, PFO, PAH/ASD, PAH/ASD, VSD, PAH/other
S4654 intron_variant DNMT1 NC_000019.10:g.10146569G>A A/G isolated CHD/non-isolated CHD: VSD/ASD/TOF/PDA/PAH/DORV/PS/AS/VSD, PFO/VSD, PFO, PAH/ASD, PAH/ASD, VSD, PAH/other
S4655 intron_variant DNMT1 NC_000019.10:g.10146569G>A A/A isolated CHD/non-isolated CHD: VSD/ASD/TOF/PDA/PAH/DORV/PS/AS/VSD, PFO/VSD, PFO, PAH/ASD, PAH/ASD, VSD, PAH/other
S4656 intron_variant DNMT1 NC_000019.10:g.10146569G>A A/G+A/A isolated CHD/non-isolated CHD: VSD/ASD/TOF/PDA/PAH/DORV/PS/AS/VSD, PFO/VSD, PFO, PAH/ASD, PAH/ASD, VSD, PAH/other
S4657 intron_variant DNMT1 NC_000019.10:g.10146569G>A A/G+G/G isolated CHD/non-isolated CHD: VSD/ASD/TOF/PDA/PAH/DORV/PS/AS/VSD, PFO/VSD, PFO, PAH/ASD, PAH/ASD, VSD, PAH/other
S4658 intron_variant DNMT1 NC_000019.10:g.10146569G>A G isolated CHD/non-isolated CHD: VSD/ASD/TOF/PDA/PAH/DORV/PS/AS/VSD, PFO/VSD, PFO, PAH/ASD, PAH/ASD, VSD, PAH/other
S4659 intron_variant DNMT1 NC_000019.10:g.10146569G>A A isolated CHD/non-isolated CHD: VSD/ASD/TOF/PDA/PAH/DORV/PS/AS/VSD, PFO/VSD, PFO, PAH/ASD, PAH/ASD, VSD, PAH/other