Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22 13
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24 13
rs2221903
IL21-AS1 ; IL21
0.752 0.360 4 122617757 intron variant C/T snv 0.77 12
rs12508721
IL21-AS1
0.742 0.360 4 122623509 intron variant C/T snv 0.24 11
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs2439302
NRG1
0.776 0.200 8 32574851 intron variant G/C snv 0.54 9
rs17849071
PIK3CA
0.776 0.160 3 179218439 intron variant T/G snv 7.9E-02 8
rs3917225
IL1R1
0.807 0.160 2 102152842 intron variant A/G snv 0.36 6
rs7850258
PTCSC2
0.827 0.200 9 97786731 intron variant A/G snv 0.72 6
rs13143866
IL21 ; IL21-AS1
0.851 0.200 4 122619603 intron variant G/A snv 0.24 4
rs1946519
IL18
0.851 0.120 11 112164784 intron variant A/C snv 0.60 4
rs7028661
PTCSC2
0.882 0.080 9 97776188 intron variant A/G snv 0.72 4
rs10951937
SUN3
0.882 0.080 7 47992027 intron variant A/C snv 0.43 3
rs12769288
MGMT
0.882 0.080 10 129488086 intron variant C/T snv 0.10 3
rs4658973
WDR3 ; SPAG17
0.882 0.080 1 117956431 intron variant T/G snv 0.34 3
rs78929565
CLOCK
0.882 0.080 4 55539035 intron variant C/A;T snv 3
rs2145418 0.882 0.080 1 118422631 intergenic variant C/A snv 0.78 3
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 11
rs6013897 0.790 0.200 20 54125940 regulatory region variant T/A snv 0.23 7
rs7037324
LOC112268051
0.882 0.080 9 97896036 regulatory region variant A/G snv 0.71 3