All of V1657

ID Consequence Gene/Location Detail Geno Type CHD Type
S3490 missense_variant MTHFR NM_005957.5:c.677T>C C isolated CHD/non-isolated CHD: NA
S3491 missense_variant MTHFR NM_005957.5:c.677T>C T isolated CHD/non-isolated CHD: NA