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. 2012 Feb 8;20(8):825–830. doi: 10.1038/ejhg.2012.13

Table 3. Clients' perceived opinions and experiences with DTC-GT.

  Client, n=25
  n (%)
Type of DTC-GT ordered
 Testing of multiple SNPs or CNVs in multiple genes 10 (40)
 Whole exome sequencing (next generation sequencing) 4 (16)
 Whole genome sequencing (next generation sequencing) 4 (16)
 Full sequencing of two or more genes 3 (12)
 Full sequencing of a single gene 2 (8)
 Testing of one or more SNPs or CNVs in a single gene 1 (4)
 Unknown 1 (4)
   
Motivation for having DTC-GT (≥1 motivation per client)
 To know their susceptibility/predisposition for complex conditions 14 (56)
 To identify monogenic conditions, including carrier testing 9 (36)
 For academic purposes (eg, interest or curiosity) 3 (12)
 For other non health-related applications (eg, ancestry, nutrigenetics, paternity testing) 1 (4)
 For pharmacogenetic uses 0 (0)
 To assess their sporting ability 0 (0)
   
Reasons given for seeking professional services in regard to their DTC-GT (≥1 reason per client)
 Needed help interpreting the results 20 (80)
 Concerned for health of family members 15 (60)
 Seeking reproductive risk information 11 (44)
 Concerned for own health 10 (40)
 Seeking information on specific conditions 10 (40)
 Seeking further genetic testing 4 (16)
 Questioning validity of DTC-GT results 2 (8)
   
Satisfaction with chosen DTC-GT service
 Very satisfied 8 (32)
 Somewhat satisfied 8 (32)
 Not satisfied 9 (36)
   
Feelings of regret for having DTC-GT
 No 14 (56)
 Yes 5 (20)
 Unknown 6 (24)

Abbreviations: CNV, copy number variation; DTC-GT, direct-to-consumer genetic testing; SNP, single-nucleotide polymorphism.