All of V1741

ID Consequence Gene/Location Detail Geno Type CHD Type
S3668 intron_variant NRP1 NC_000010.11:g.33335167C>T C/C isolated CHD: TOF
S3669 intron_variant NRP1 NC_000010.11:g.33335167C>T C/T isolated CHD: TOF
S3670 intron_variant NRP1 NC_000010.11:g.33335167C>T T/T isolated CHD: TOF
S3671 intron_variant NRP1 NC_000010.11:g.33335167C>T T isolated CHD: TOF