Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs2665390
LOC107986148 ; TIPARP
0.776 0.160 3 156679960 intron variant C/T snv 0.92 8
rs6005807
TTC28 ; LOC101929594
0.925 0.120 22 28538325 intron variant T/C snv 0.89 2
rs1950902
MTHFD1
0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs7969255
PRANCR
1.000 0.120 12 70148026 intron variant T/G snv 0.82 1
rs2227564
PLAU ; C10orf55
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 15
rs150303591
FRAS1
1.000 0.120 4 78088155 intron variant C/T snv 0.80 1
rs2191249
BRIP1
0.882 0.120 17 61758503 intron variant T/G snv 0.79 3
rs711830
HAGLR ; HOXD3
0.882 0.120 2 176172583 3 prime UTR variant A/C;G;T snv 0.76 3
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 9
rs851797
EXO1
0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17
rs6134303 1.000 0.120 20 11586401 intergenic variant T/G snv 0.67 1
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs17693104
SH2D4B
1.000 0.120 10 80608465 intron variant T/C snv 0.61 1
rs1467465
THEMIS2
0.827 0.160 1 27884892 non coding transcript exon variant A/G snv 0.61 7
rs351771
APC
0.882 0.120 5 112828864 synonymous variant G/A snv 0.65 0.59 3
rs230521
NFKB1
0.851 0.160 4 102542171 intron variant C/G snv 0.59 4
rs7953249
HNF1A-AS1
0.882 0.160 12 120965921 splice region variant G/A snv 0.59 4
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs3923087
AXIN2
0.827 0.160 17 65553143 intron variant T/C snv 0.58 5
rs1836724
ERBB4
0.807 0.240 2 211380227 3 prime UTR variant G/A snv 0.57 6