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Table 1 Distribution of causal minor alleles of Q1 and Q2 in the eight simulated pedigrees

From: Enriching rare variants using family-specific linkage information

Gene

Family

Founder

 

1

2

3

4

5

6

7

8

Yes

No

Q1

          

 ARNT

3

2

0

0

6

0

0

0

4

7

 ELAVL4*

0

0

1

0

0

0

0

0

1

0

 FLT1

0

0

5

0

28

16

13

12

28

46

 FLT4

0

0

0

0

0

0

0

0

0

0

 HIF1A*

0

0

0

0

1

0

0

0

1

0

 HIF3A*

0

0

0

0

3

0

0

0

1

2

 KDR

14

37

43

31

6

0

93

0

55

169

 VEGFA*

4

20

0

0

0

0

22

0

3

43

 VEGFC*

0

0

0

0

0

0

31

0

1

30

Q2

          

 BCHE

4

0

0

0

1

0

2

2

5

4

 GCKR*

2

0

0

0

0

0

0

0

1

1

 INSIG1

0

0

0

0

0

0

0

0

0

0

 LPL

7

20

2

1

0

1

23

7

15

46

 PDGFD*

0

0

0

0

0

0

2

0

1

1

 PLAT

0

1

2

0

0

3

0

0

4

2

 RARB

0

0

0

0

0

0

0

0

0

0

 SIRT1

0

0

3

0

0

4

21

0

4

24

 SREBF1

16

21

0

5

9

12

8

0

13

58

 VLDLR

2

0

0

0

11

0

6

0

4

15

 VNN1

35

60

27

15

24

17

77

0

54

201

 VNN3

24

17

27

0

21

0

42

42

46

127

 VWF

0

0

0

2

0

0

0

0

2

0

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