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Table 1 The number of variants in each gene in family-based, population-based, and combined data sets

From: On combining family- and population-based sequencing data

Gene

Number of variants

Number of causal variants

Totala

Familyb

Populationc

Combinedd

DBP

  MAP4

41

5

8

8

  TNN

52

11

15

15

  NRF1

17

0

0

0

  LEPR

43

3

7

7

  FLT3

46

1

2

2

  ZFP37

18

1

5

5

  CGN

56

9

16

16

  MTRR

62

6

10

10

  SLC35E2

29

0

0

0

  ZNF443

20

1

5

5

  RAI1

55

3

7

7

  PTTG1IP

47

0

0

0

  CABP2

37

1

0

1

  ZNF544

34

3

3

3

  REPIN1

32

3

4

4

SBP

  MAP4

41

5

9

9

  TNN

52

12

15

15

  NRF1

17

0

0

0

  LEPR

43

3

7

7

  FLT3

46

1

2

2

  ZNF443

20

1

5

5

  CABP2

37

1

0

1

  GTF2IRD1

34

0

0

0

  FLNB

81

5

7

7

  GSN

39

2

7

7

  LRP8

35

1

2

2

  PSMD5

33

2

4

4

  GAB2

77

1

2

2

  ABTB1

42

1

1

1

  KRTAD11-1

4

0

0

0

  1. aThe number of variants that have the same position between the family- and population-based data
  2. bThe number of causal variants of the intersected variants in the family-based data
  3. cThe number of causal variants of the intersected variants in the population-based data
  4. dThe number of causal variants of the intersected variants in the combined data between the family- and population-based data