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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