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. Author manuscript; available in PMC: 2008 Mar 24.
Published in final edited form as: Am J Med Genet A. 2007 May 1;143(9):961–970. doi: 10.1002/ajmg.a.31575

TABLE II.

Coding Frequencies by Sample Set, N (%)

Variables coded Clinical sample set (N=131) Genetic sample set (N=102) General sample (set N=97) Total (N=330)
Basic features
 Hypothesis 50 (38.2) 21 (20.6) 28 (28.9) 99 (30.0)
 Limitations 46 (35.1) 12 (11.8) 17 (17.5) 75 (22.7)
 Sample origin 93 (71.0) 58 (56.9) 55 (56.7) 206 (62.4)
Reason for using population
 Basis for assigning population label 13 (9.9) 9 (8.8) 8 (8.2) 30 (9.1)
 Why this population 17 (13.0) 12 (11.8) 8 (8.2) 37 (11.2)
 Why population 17 (13.0) 9 (8.8) 10 (10.3) 36 (10.9)
Ways of using race and ethnicity terms
 No term 22 (16.8) 14 (13.7) 15 (15.5) 51 (15.5)
 Reference population only 18 (13.7) 5 (4.9) 10.3% (10) 10.0% (33)
 Sample population only 26 (19.8) 30 (29.4) 20 (20.6) 76 (23.0)
 Independent variable 61 (46.6) 46 (45.1) 47 (48.5) 154 (46.7)
 Dependent variable 4 (3.1) 7 (6.9) 5 (5.2) 16 (4.8)
 DNA with label 3 (2.3) 22 (21.6) 10 (10.3) 35 (10.6)
 Defines race or ethnicity 0 (0.00) 0 (0.00) 0 (0.00) 0 (0.00)