Skip to main content

Table 2 Linkage and association analyses in all 200 replicates

From: Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data

Gene

Causal SV

MAF

β a

Merlin-VC

ROMP

ASSOC

Q1

      

FLT1

c13s431

0.0172

0.7414

 

1 (0.5%)

32 (16%)

FLT1

c13s523

0.0667

0.6500

 

7 (3.5%)

75 (37.5%)

FLT1

CSVb

    

1 (0.5%)

KDR

c4s1878

0.1650

0.1357

 

18 (9%)

10 (5%)

KDR

c4s1884

0.0208

0.2956

 

2 (1%)

 

VEGFC

c4s4935

0.0007

1.3573

13 (6.5%)

200 (100%)

200 (100%)

VEGFA

c6s2981

0.0022

1.2065

50 (25%)

200 (100%)

200 (100%)

Q2

      

LPL

c8s442

0.01578

0.49459

 

11 (5.5%)

15 (7.5%)

SIRT1

c10s3109

0.00072

0.51421

 

4 (2%)

 

SREBF1

c17s1043

0.0043

0.49941

 

2 (1%)

4 (2%)

VLDLR

CSVb

   

4 (2%)

1 (0.5%)

VNN1

c6s5380

0.17073

0.24437

 

4 (2%)

10 (5%)

VNN3

c6s5441

0.09828

0.27053

 

1 (0.5%)

3 (1.5%)

  1. Number (%) of replicates are shown where the test achieved genome-wide significance. ASSOC and ROMP results are presented for collapsing definition 2 (MAF < 1% and nonsynonymous SV).
  2. a Effect size of SV on quantitative trait [1].
  3. b Multiple causal variants exist in this gene’s collapsed sequence variant.