All of V1597

ID Consequence Gene/Location Detail Geno Type CHD Type
S3337 missense_variant NFATC1 NM_006162.5:c.2251T>G T isolated CHD/non-isolated CHD: NA
S3338 missense_variant NFATC1 NM_006162.5:c.2251T>G G isolated CHD/non-isolated CHD: NA