All of V0742

ID Consequence Gene/Location Detail Geno Type CHD Type
S1706 intron_variant NOS3 NM_000603.5:c.3106+11G>T T/T isolated CHD: ASD
S1707 intron_variant NOS3 NM_000603.5:c.3106+11G>T G/G+G/T isolated CHD: ASD