All of V2166

ID Consequence Gene/Location Detail Geno Type CHD Type
S3999 synonymous_variant HOXB1 NM_002144.4:c.450G>A G/G isolated CHD: DORV
S4000 synonymous_variant HOXB1 NM_002144.4:c.450G>A G/A isolated CHD: DORV
S4001 synonymous_variant HOXB1 NM_002144.4:c.450G>A A/A isolated CHD: DORV