All of V1738

ID Consequence Gene/Location Detail Geno Type CHD Type
S3656 intron_variant NRP1 NC_000010.11:g.33206339C>T T/T isolated CHD: TOF
S3657 intron_variant NRP1 NC_000010.11:g.33206339C>T C/T isolated CHD: TOF
S3658 intron_variant NRP1 NC_000010.11:g.33206339C>T C/C isolated CHD: TOF
S3659 intron_variant NRP1 NC_000010.11:g.33206339C>T C isolated CHD: TOF