Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35599367
CYP3A4
1.000 0.080 7 99768693 intron variant G/A snv 3.2E-02 2
rs121918529
MEF2A
0.882 0.080 15 99690400 missense variant C/T snv 6.1E-04 6.5E-04 3
rs2895811
HHIPL1
0.851 0.080 14 99667605 intron variant T/A;C snv 4
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1012841819
ADRA2B
0.882 0.160 2 96115728 missense variant G/A snv 4.0E-06 4
rs2540487
LTA4H
1.000 0.080 12 96036005 intron variant C/A;G;T snv 1
rs2247570
LTA4H
1.000 0.080 12 96028599 intron variant T/C snv 0.33 1
rs541811
UGGT2
1.000 0.080 13 96019856 intron variant G/C;T snv 1
rs12026
PON2
0.827 0.240 7 95411704 missense variant G/C snv 0.27 0.27 6
rs7493
PON2
0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1058932
CYP2C8
1.000 0.080 10 95037104 3 prime UTR variant G/A snv 0.22 0.24 1
rs1361600
MIR12133 ; F3
0.925 0.120 1 94542362 upstream gene variant C/T snv 0.51 3
rs774688955
F3
1.000 0.080 1 94541666 5 prime UTR variant G/A;T snv 1
rs1324214
F3
0.925 0.120 1 94531732 intron variant G/A snv 0.21 3
rs3354
F3
1.000 0.080 1 94530263 3 prime UTR variant C/A;G;T snv 0.28 1
rs3917639 0.925 0.120 1 94527220 downstream gene variant C/T snv 2
rs42524
COL1A2
0.827 0.160 7 94413927 missense variant C/A;G;T snv 8.0E-06; 0.77; 8.0E-06 6
rs16936752
WNK2
0.925 0.120 9 93301408 intron variant T/G snv 8.3E-02 2
rs2295394
ITPK1
1.000 0.080 14 92946398 synonymous variant G/A snv 8.4E-02 7.3E-02 1
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2270461
TCF25
1.000 0.080 16 89905937 intron variant T/C snv 0.23 1
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 9