All of V0602

ID Consequence Gene/Location Detail Geno Type CHD Type
S1432 missense_variant MTHFR NM_005957.5:c.677T>C C/C NA: Septa and valve abnormalities
S1433 missense_variant MTHFR NM_005957.5:c.677T>C C/T NA: Septa and valve abnormalities
S1434 missense_variant MTHFR NM_005957.5:c.677T>C T/T NA: Septa and valve abnormalities
S1435 missense_variant MTHFR NM_005957.5:c.677T>C C/T+T/T NA: Septa and valve abnormalities