All of V2370

ID Consequence Gene/Location Detail Geno Type CHD Type
S4660 intron_variant DNMT1 NC_000019.10:g.10189741A>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
S4661 intron_variant DNMT1 NC_000019.10:g.10189741A>G 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
S4662 intron_variant DNMT1 NC_000019.10:g.10189741A>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
S4663 intron_variant DNMT1 NC_000019.10:g.10189741A>G 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
S4664 intron_variant DNMT1 NC_000019.10:g.10189741A>G 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
S4665 intron_variant DNMT1 NC_000019.10:g.10189741A>G 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
S4666 intron_variant DNMT1 NC_000019.10:g.10189741A>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