All of V2164

ID Consequence Gene/Location Detail Geno Type CHD Type
S3996 missense_variant HOXB1 NM_002144.4:c.309A>T A/A isolated CHD: Pm VSD
S3997 missense_variant HOXB1 NM_002144.4:c.309A>T A/T isolated CHD: Pm VSD