All of V0192

ID Consequence Gene/Location Detail Geno Type CHD Type
S0508 missense_variant MTHFR NM_005957.5:c.677T>C C/C isolated CHD: HLHS/TOF/DORV/TGV/EA/VSD/PS/CoA/ASD
S0509 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD: HLHS/TOF/DORV/TGV/EA/VSD/PS/CoA/ASD
S0510 missense_variant MTHFR NM_005957.5:c.677T>C T/T isolated CHD: HLHS/TOF/DORV/TGV/EA/VSD/PS/CoA/ASD
S0511 missense_variant MTHFR NM_005957.5:c.677T>C C/C isolated CHD: HLHS/TOF/DORV/TGV/EA/VSD/PS/CoA/ASD
S0512 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD: HLHS/TOF/DORV/TGV/EA/VSD/PS/CoA/ASD
S0513 missense_variant MTHFR NM_005957.5:c.677T>C T/T isolated CHD: HLHS/TOF/DORV/TGV/EA/VSD/PS/CoA/ASD
S0514 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD: HLHS/TOF/DORV/TGV/EA/VSD/PS/CoA/ASD
S0515 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD: HLHS/TOF/DORV/TGV/EA/VSD/PS/CoA/ASD