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. Author manuscript; available in PMC: 2018 Mar 1.
Published in final edited form as: Pediatr Nephrol. 2016 Oct 20;32(3):467–476. doi: 10.1007/s00467-016-3513-3

Table 5.

Analysis of burden of at least one variant in any of the 21 monogenic nephrotic syndrome (NS) genes in clinically defined subgroup of participants. Statistical analysis was performed using two-tailed Fisher’s exact test.

p-value

Pediatric NS vs 1000G Ped NS (n=98) 1000G (n=2498)
 Stringent Filter 12 (12%) 384 (15%) 0.48
 Relaxed Filter 57 (58%) 1699 (68%) 0.04

Pediatric FSGS vs 1000G Ped FSGS (n=30) 1000G (n=2498)
 Stringent Filter 2 (7%) 384 (15%) 0.3
 Relaxed Filter 14 (47%) 1699 (68%) < 0.01

Pediatric MCD vs 1000G Ped MCD (n=44) 1000G (n=2498)
 Stringent Filter 8 (18%) 384 (15%) 0.53
 Relaxed Filter 35 (80%) 1699 (68%) 0.14

Pediatric Complete Remission History Yes CR (n=63) No CR (n=35)
 Stringent Filter 8 (67%) 4 (33%) 0.22
 Relaxed Filter 38 (66%) 20 (33%) 0.01

Pediatric FSGS vs Pediatric MCD Pediatric FSGS (n=30) Pediatric MCD (n=44)
 Stringent Filter 2 (7%) 8 (18%) 0.19
 Relaxed Filter 14 (47%) 35 (80%) < 0.01

FSGS+MCD vs 1000G FSGS+MCD (n=162) 1000G (n=2498)
 Stringent Filter 23 (14%) 384 (15%) 0.82
 Relaxed Filter 108 (58%) 1699 (68%) 0.73

FSGS + MCD (Ped) vs 1000G FSGS+MCD (n=74) 1000G (n=2498)
 Stringent Filter 10 (14%) 384 (15%) 0.75
 Relaxed Filter 49 (58%) 1699 (68%) 0.8

Abbreviations are as follows: Ped = Pediatric, MCD= minimal change disease, FSGS= focal segmental glomerulosclerosis, CR = Complete Remission.