Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1899663
HOTAIR
0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs2424913
DNMT3B
0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs2107425
MRPL23 ; H19
0.732 0.280 11 1999845 intron variant C/T snv 16
rs11954856
APC
0.732 0.200 5 112751630 intron variant T/G snv 0.54 12
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 11
rs2699887
PIK3CA ; LOC101928739
0.763 0.280 3 179148620 intron variant C/T snv 0.18 11
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 9
rs1256031
ESR2
0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 9
rs4648068
NFKB1
0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs11655505
NBR2 ; BRCA1
0.776 0.160 17 43126360 intron variant G/A snv 0.31 8
rs1989839
ZMYND10 ; RASSF1
0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20 8
rs2665390
LOC107986148 ; TIPARP
0.776 0.160 3 156679960 intron variant C/T snv 0.92 8
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 7
rs1469713
GATAD2A
0.827 0.160 19 19417997 intron variant A/G snv 0.44 7
rs7937840
INCENP
0.807 0.200 11 62126500 intron variant C/T snv 0.20 7