All of V1849

ID Consequence Gene/Location Detail Geno Type CHD Type
S3852 missense_variant MTHFD1 NM_005956.4:c.1958G>A G/G isolated CHD: ASD
S3853 missense_variant MTHFD1 NM_005956.4:c.1958G>A G/A+A/A isolated CHD: ASD

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