Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2504106
DAAM2
0.925 0.120 6 39854343 intron variant A/G snv 0.61 2
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs1259293
FSTL1
0.925 0.120 3 120421014 intron variant T/C snv 0.59 2
rs9582036
FLT1
0.776 0.280 13 28311271 intron variant C/A snv 0.59 8
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs2761016
ALAD
0.925 0.120 9 113391072 intron variant T/C snv 0.59 2
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs1642742
VHL
1.000 0.120 3 10150259 3 prime UTR variant G/A snv 0.57 1
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs7579899
EPAS1
0.925 0.120 2 46310465 intron variant A/G snv 0.52 2
rs4381241
FAF1
0.925 0.120 1 50441766 intron variant T/C snv 0.51 2
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs7102764
GRM5
0.925 0.120 11 88778092 intron variant A/T snv 0.50 2
rs2854744
IGFBP3
0.695 0.520 7 45921476 intron variant G/T snv 0.48 20
rs1802073
SFRP4 ; EPDR1
0.851 0.240 7 37907562 missense variant G/T snv 0.44 0.45 4
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs6442260
ATG7
0.925 0.160 3 11549277 intron variant G/A snv 0.42 2
rs8106822
LOC107985311
0.925 0.120 19 31373516 intron variant G/A snv 0.42 2
rs34048824
DNMT3A
1.000 0.120 2 25312674 intron variant T/C snv 0.42 1
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs9679290
EPAS1
0.925 0.120 2 46330505 intron variant G/C snv 0.41 2
rs10771279
ITPR2
0.925 0.120 12 26377610 intron variant T/A;C snv 0.40 2