All of V1435

ID Consequence Gene/Location Detail Geno Type CHD Type
S2931 intron_variant FIGN NC_000002.12:g.163641436C>G C/G+G/G isolated CHD: TOF
S2932 intron_variant FIGN NC_000002.12:g.163641436C>G C/C+G/G isolated CHD: TOF