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. Author manuscript; available in PMC: 2019 Jun 1.
Published in final edited form as: J Genet Couns. 2017 Nov 22;27(3):709–722. doi: 10.1007/s10897-017-0172-x

Table 1.

Demographics of participants by study group (n=192).

Demographics ES w/PDR (n=40) ES no PDR (n=67) No ES (n=85) p-value
 Female 73% 66% 84% 0.038
 Married 90% 88% 83% 0.530
Age
 Mean ± SD (range) 50 ± 13.6 (33–79) 50 ± 14.6 (22–84) 48 ± 14.2 (23–88) 0.600
Ethnicity and Race
 White, Non-Hispanic 80% 88% 81% 0.431
Education
 Up to HS or vocational training 8% 11% 16% 0.740
 Some college/Associate degree 15% 22% 19%
 College degree 33% 27% 26%
 Advanced degree 45% 40% 39%
Employment
 Employed (full or part-time) 68% 67% 59% 0.480
Current Religion (n=191)
 Christian 58% 47% 41% 0.473
 Jewish 20% 26% 38%
 Other (Buddhist, Taoist, Meditation) or >1 religion 5% 6% 5%
 None 18% 21% 16%
Parent study type
 Breast cancer 28% 30% 36% 0.011
 CHD 45% 49% 24%
 CDH, DD, D, MCA, MW, ES 28% 21% 40%
Disease status (n=184)
 Personally affected 33% 43% 46% 0.404
Children (n=191)
 Affected children 70% 58% 50% 0.143
 Unaffected children only 30% 34% 39%
 No children 0% 8% 11%

Abbreviations: congenital heart disease (CHD), congenital diaphragmatic hernia (CDH), developmental delay (DD), diabetes (D), multiple congenital anomalies (MCA), muscle weakness (MW), exome sequencing study (ES), personal disease risk (PDR).

p-values were calculated by Chi-squared test or ANOVA (age variable)