All of V0057

ID Consequence Gene/Location Detail Geno Type CHD Type
S0219 missense_variant MTHFR NM_005957.5:c.677T>C C/C isolated CHD: ASD/VSD/AVSD/AC/AS/EA/PS/PDA/TOF
S0220 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD: ASD/VSD/AVSD/AC/AS/EA/PS/PDA/TOF
S0221 missense_variant MTHFR NM_005957.5:c.677T>C T/T isolated CHD: ASD/VSD/AVSD/AC/AS/EA/PS/PDA/TOF
S0222 missense_variant MTHFR NM_005957.5:c.677T>C C/C isolated CHD: ASD/VSD/AVSD/AC/AS/EA/PS/PDA/TOF
S0223 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD: ASD/VSD/AVSD/AC/AS/EA/PS/PDA/TOF
S0224 missense_variant MTHFR NM_005957.5:c.677T>C T/T isolated CHD: ASD/VSD/AVSD/AC/AS/EA/PS/PDA/TOF
S0225 missense_variant MTHFR NM_005957.5:c.677T>C C/C isolated CHD: ASD/VSD/AVSD/AC/AS/EA/PS/PDA/TOF
S0226 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD: ASD/VSD/AVSD/AC/AS/EA/PS/PDA/TOF
S0227 missense_variant MTHFR NM_005957.5:c.677T>C T/T isolated CHD: ASD/VSD/AVSD/AC/AS/EA/PS/PDA/TOF