Carrier  Detection  (Sanger and  Family Sequencing) is a  genetic  test  used  to  identify  individuals  who carry a specific pathogenic variant without showing symptoms.   It   verifies   the   presence   of    known mutations in the individual or their family   members. This testing  is  essential  for  assessing  inheritance risks and family planning. Accurate  detection  helps guide   genetic   counseling  and   informed   clinical decisions.