All of V1430

ID Consequence Gene/Location Detail Geno Type CHD Type
S2905 intron_variant FIGN NC_000002.12:g.163641436C>G G/G NA: NA
S2906 intron_variant FIGN NC_000002.12:g.163641436C>G C/G NA: NA
S2907 intron_variant FIGN NC_000002.12:g.163641436C>G C/C NA: NA
S2908 intron_variant FIGN NC_000002.12:g.163641436C>G C/G+C/C NA: NA
S2909 intron_variant FIGN NC_000002.12:g.163641436C>G C/G+G/G NA: NA
S2910 intron_variant FIGN NC_000002.12:g.163641436C>G C/C+G/G NA: NA
S2911 intron_variant FIGN NC_000002.12:g.163641436C>G G/G NA: NA
S2912 intron_variant FIGN NC_000002.12:g.163641436C>G C/G NA: NA
S2913 intron_variant FIGN NC_000002.12:g.163641436C>G C/C NA: NA
S2914 intron_variant FIGN NC_000002.12:g.163641436C>G C/G+C/C NA: NA
S2915 intron_variant FIGN NC_000002.12:g.163641436C>G C/G+G/G NA: NA
S2916 intron_variant FIGN NC_000002.12:g.163641436C>G C/C+G/G NA: NA
S2917 intron_variant FIGN NC_000002.12:g.163641436C>G G/G NA: NA
S2918 intron_variant FIGN NC_000002.12:g.163641436C>G C/G NA: NA
S2919 intron_variant FIGN NC_000002.12:g.163641436C>G C/C NA: NA
S2920 intron_variant FIGN NC_000002.12:g.163641436C>G C/G+C/C NA: NA
S2921 intron_variant FIGN NC_000002.12:g.163641436C>G C/G+G/G NA: NA
S2922 intron_variant FIGN NC_000002.12:g.163641436C>G C/C+G/G NA: NA