Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs3864785 1.000 0.080 9 7603506 intergenic variant G/C snv 0.89 1
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs1896295
BCL11A
1.000 0.080 2 60496951 intron variant T/C snv 0.81 2
rs1896296
BCL11A
1.000 0.080 2 60496952 intron variant G/T snv 0.80 2
rs766432
BCL11A
0.925 0.080 2 60492835 intron variant C/A snv 0.80 6
rs7952106 1.000 0.080 11 113553836 regulatory region variant G/T snv 0.71 2
rs11886868
BCL11A
0.752 0.280 2 60493111 intron variant C/T snv 0.65 12
rs7584113
BCL11A
1.000 0.080 2 60494176 intron variant A/G snv 0.64 2
rs10172646
BCL11A
1.000 0.080 2 60493622 intron variant G/A snv 0.64 2
rs7557939
BCL11A
1.000 0.080 2 60494212 intron variant G/A snv 0.64 2
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs2445284 1.000 0.080 11 5008473 downstream gene variant C/T snv 0.57 1
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs10793902
LOC105376294
1.000 0.080 9 130502523 downstream gene variant C/T snv 0.52 1
rs6545816
BCL11A
1.000 0.080 2 60487726 intron variant A/C;G snv 0.50 2
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs6545817
BCL11A
1.000 0.080 2 60488044 intron variant C/T snv 0.49 2
rs6729815
BCL11A
1.000 0.080 2 60496537 intron variant T/C snv 0.49 4
rs7948471
HBE1 ; HBG2 ; OR51B5 ; OR51I2
1.000 0.080 11 5450516 intron variant G/A snv 0.47 1
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249