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Table 3 Percentage of phenotypic variance explained by causal genes of Q1 and Q2 in the eight simulated pedigrees

From: Enriching rare variants using family-specific linkage information

Gene

Family

Total samples

 

1

2

3

4

5

6

7

8

 

Q1

         

 ARNT

1.3

0.1

0

0

2.0

0

0

0

0.3

 ELAVL4*

0

0

0.8

0

0

0

0

0

0.08

 FLT1

0

0

1.4

0

22.2

11.9

2.3

14.6

5.8

 FLT4

0

0

0

0

0

0

0

0

0

 HIF1A*

0

0

0

0

0.07

0

0

0

0.006

 HIF3A*

0

0

0

0

0.4

0

0

0

0.04

 KDR

0.8

1.6

0.9

1.8

0.5

0

1.6

0

1.2

 VEGFA*

7.9

24.6

0

0

0

0

14.6

0

9.0

 VEGFC*

0

0

0

0

0

0

23.8

0

7.9

Q2

         

 BCHE

2.4

0

0

0

0.07

0

0.06

0.2

0.3

 GCKR*

0.3

0

0

0

0

0

0

0

0.04

 INSIG1

0

0

0

0

0

0

0

0

0

 LPL

1.8

4.1

0.6

0.4

0

0.3

4.3

2.2

2.1

 PDGFD*

0

0

0

0

0

0

0.5

0

0.1

 PLAT

0

0.02

0.7

0

0

0.08

0

0

0.1

 RARB

0

0

0

0

0

0

0

0

0

 SIRT1

0

0

1.0

0

0

4.2

3.4

0

1.3

 SREBF1

3.8

2.2

0

1.2

2.1

3.0

1.2

0

1.7

 VLDLR

0.6

0

0

0

4.6

0

3.1

0

1.2

 VNN1

1.6

2.8

1.8

1.4

1.7

1.3

2.1

0

1.9

 VNN3

1.7

1.2

1.9

0

1.6

0

2.1

7.8

2.2

 VWF

0

0

0

1.7

0

0

0

0

0.2

  1. Asterisks indicate a single nonmonomorphic causal variant in the gene.