Table 2 Mutation spectrum of recessive NOD2 variants in the RGC-GHS DiscovEHR adult IBD cohort.

From: Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn’s Disease

NOD2 variants

# IBD patients

Mean age (range)

# CD Dx

% CD Dx

# Male

% Male

# Perianal

% Perianal

Homozygous

 p.R702W

10

47.3 (16.0–76.3)

10

100

5

50.0

1

10.0

 p.G908R

0

 p.L1007fs

8

40.25 (11.0–75.0)

8

100

4

50.0

3

37.5

Compound heterozygous

Common/common

 p.R702W/p.G908R

6

48.5 (11.4–54.2)

3

50.0

5

83.3

1

16.7

 p.R702W/p.L1007fs

11

38.5 (21.5–69.2)

8

72.7

3

27.3

2

18.2

 p.G908R/p.L1007fs

5

35.2 (20.0–52.4)

4

80.0

2

40.0

0

0.0

Common/rare

16

40.3 (10.8–66.1)

8

50.0

8

50.0

6

37.5

Rare/rare

8

60.9 (30.8–78.7)

4

50.0

3

37.5

1

12.5

  1. Common NOD2 variants refer to the three main low-frequency Crohn’s Disease risk variants p.R702W, p.G908R, and p.L1007fs; Rare NOD2 variants refer to other low-frequency variants (MAF ≤ 5%).
  2. Dx, diagnosis.