All of V1433

ID Consequence Gene/Location Detail Geno Type CHD Type
S2927 intron_variant FIGN NC_000002.12:g.163641436C>G C/G+G/G isolated CHD: ASD
S2928 intron_variant FIGN NC_000002.12:g.163641436C>G C/C+G/G isolated CHD: ASD

All rights reserved: Center for Systems Biology, Soochow University