All of V0069

ID Consequence Gene/Location Detail Geno Type CHD Type
S0325 missense_variant MTHFR NM_005957.5:c.677T>C C/C isolated CHD: TOF/HLHS/TGA/VSD/AVS/CoA/PS
S0326 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD: TOF/HLHS/TGA/VSD/AVS/CoA/PS
S0327 missense_variant MTHFR NM_005957.5:c.677T>C T/T isolated CHD: TOF/HLHS/TGA/VSD/AVS/CoA/PS
S0328 missense_variant MTHFR NM_005957.5:c.677T>C C/C isolated CHD: TOF/HLHS/TGA/VSD/AVS/CoA/PS
S0329 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD: TOF/HLHS/TGA/VSD/AVS/CoA/PS
S0330 missense_variant MTHFR NM_005957.5:c.677T>C T/T isolated CHD: TOF/HLHS/TGA/VSD/AVS/CoA/PS