All of V1658

ID Consequence Gene/Location Detail Geno Type CHD Type
S3492 missense_variant MTHFR NM_005957.5:c.1298A>C A isolated CHD/non-isolated CHD: NA
S3493 missense_variant MTHFR NM_005957.5:c.1298A>C C isolated CHD/non-isolated CHD: NA

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