All of V2368

ID Consequence Gene/Location Detail Geno Type CHD Type
S4646 missense_variant DNMT1 NM_001379.4:c.931A>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
S4647 missense_variant DNMT1 NM_001379.4:c.931A>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
S4648 missense_variant DNMT1 NM_001379.4:c.931A>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
S4649 missense_variant DNMT1 NM_001379.4:c.931A>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
S4650 missense_variant DNMT1 NM_001379.4:c.931A>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
S4651 missense_variant DNMT1 NM_001379.4:c.931A>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
S4652 missense_variant DNMT1 NM_001379.4:c.931A>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