Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2606345
CYP1A1
0.732 0.360 15 74724835 intron variant C/A snv 0.46 16
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5
rs3774934
NFKB1
0.851 0.080 4 102506319 intron variant A/C;G;T snv 4
rs7692976
EGF
1.000 0.040 4 109990411 intron variant A/G;T snv 2
rs10905928
CELF2
1.000 0.040 10 11300924 intron variant C/A snv 0.21 1
rs1190286
POPDC3 ; BVES-AS1
1.000 0.040 6 105163071 intron variant C/T snv 0.66 1
rs13402990
C2orf42 ; TIA1
1.000 0.040 2 70231632 intron variant A/T snv 9.7E-03 1
rs2298991
EGF
1.000 0.040 4 109970856 intron variant T/A;G snv 1
rs2515475
ANGPT2 ; MCPH1
1.000 0.040 8 6530918 intron variant C/T snv 0.19 1
rs2592178
C2orf42 ; TIA1
1.000 0.040 2 70245350 intron variant G/A snv 0.27 1
rs516651
EGLN1
1.000 0.040 1 231406910 intron variant C/T snv 0.15 1
rs6533485
EGF
1.000 0.040 4 110006407 intron variant G/C snv 0.61 1
rs672961
LRRC7
1.000 0.040 1 70101505 intron variant C/G snv 0.99 1
rs7068124
CELF2
1.000 0.040 10 11023453 intron variant T/C;G snv 1
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs1800450
MBL2
0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs149989682
ABCA3
0.790 0.240 16 2317763 missense variant T/A;C snv 2.3E-03 10
rs315952
IL1RN
0.763 0.400 2 113132727 missense variant T/A;C snv 4.0E-06; 0.31 10
rs1130866
SFTPB
0.827 0.160 2 85666618 missense variant G/A;C snv 0.50 9
rs1805018
PLA2G7
0.827 0.200 6 46711566 missense variant A/G snv 6.8E-02 0.10 6