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. 2020 May 7;11:464. doi: 10.3389/fgene.2020.00464

Table 2.

Patient groups and positives for pathogenic/likely pathogenic variants in PKD1/PKD2.

All (n = 212) Validation cohort (n = 21) Confirmation cohort (n = 36) Discovery cohort (n = 155)
n % n % n % n %
PKD1/PKD2 Positive 138 65.1 21 100.0 31 86.1 86 55.5
ADPKD-PKD1 118 85.5 18 85.7 28 90.3 72 83.7
  ADPKD-PKD1T 92 78.0 12 66.7 25 89.3 55 76.4
  ADPKD-PKD1NT 26 22.0 6 33.3 3 10.7 17 23.6
ADPKD-PKD2 20 14.5 3 14.3 3 9.7 14 16.3
PKD1/PKD2 Negative 74 34.9 0 0.0 5 13.9 69 44.5
 PKD1/2 VUS 24 11.3 0 0.0 3 8.3 21 13.5
  ADPKD-PKD1VUS 21 87.5 0 0.0 3 100.0 18 85.7
  ADPKD-PKD2VUS 3 12.5 0 0.0 0 0.0 3 14.3

One proband, homozygous for a hypomorphic PKD1 variant, is also included among the positives. Patients showing variants of uncertain significance (VUS) are also reported and included among the negatives. T, protein truncating; NT, protein non-truncating.