Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs6166
FSHR
0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 17
rs732774
ATP7B
0.827 0.320 13 51949672 missense variant C/T snv 0.57 0.56 5
rs11954856
APC
0.732 0.200 5 112751630 intron variant T/G snv 0.54 12
rs9375701
L3MBTL3
0.827 0.160 6 130062912 intron variant C/T snv 0.53 6
rs2424913
DNMT3B
0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 9
rs2180314
GSTA2
0.776 0.200 6 52752933 missense variant C/G snv 0.60 0.52 8
rs638820
GSTM4 ; GSTM2
0.827 0.160 1 109667284 intron variant G/A snv 0.52 5
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 11
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs2363956
ANKLE1
0.776 0.160 19 17283315 missense variant T/G snv 0.48 0.50 8
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs2516839
USF1
0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 14
rs12373237
LAMA3
0.851 0.200 18 23845972 intron variant G/A snv 0.47 5
rs7260002
CGB5
0.882 0.120 19 49042615 non coding transcript exon variant A/C;G snv 0.46 3
rs2708861
HUS1
0.851 0.120 7 47977120 intron variant T/G snv 0.46 6
rs7206411
CMIP
1.000 0.120 16 81619883 non coding transcript exon variant T/C snv 0.45 1
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1791890
LOC107984393
1.000 0.120 11 116120763 intergenic variant A/G snv 0.44 1
rs11973028
JAZF1
1.000 0.120 7 27853217 intron variant C/T snv 0.44 1
rs1469713
GATAD2A
0.827 0.160 19 19417997 intron variant A/G snv 0.44 7
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 18