All of V0699

ID Consequence Gene/Location Detail Geno Type CHD Type
S1611 intron_variant RPH3A NC_000012.12:g.112602139C>T T/T isolated CHD: ASD
S1612 intron_variant RPH3A NC_000012.12:g.112602139C>T T/C isolated CHD: ASD
S1613 intron_variant RPH3A NC_000012.12:g.112602139C>T C/C isolated CHD: ASD