Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs647161
C5orf66
0.776 0.080 5 135163402 intron variant C/A snv 0.63 10
rs822395
ADIPOQ
0.776 0.240 3 186849018 intron variant C/A;G snv 10
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 9
rs7421861
LOC105373977 ; PDCD1
0.790 0.200 2 241853198 intron variant A/G;T snv 9
rs7727691
XRCC4 ; TMEM167A
0.763 0.200 5 83075876 intron variant C/T snv 0.32 9
rs7904519
TCF7L2
0.763 0.240 10 113014168 intron variant A/G snv 0.55 9
rs9288518
XRCC5
0.776 0.240 2 216196997 intron variant A/G snv 0.35 9
rs2302615
ODC1-DT ; SNORA80B ; ODC1
0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs2735971
MRPL23 ; H19
0.790 0.240 11 2000419 intron variant T/C snv 7
rs4464148
SMAD7
0.827 0.120 18 48932662 intron variant T/C snv 0.25 7
rs115797771
KLF5
0.807 0.080 13 73064505 intron variant A/C snv 5.8E-02 6
rs1990172
MACC1
0.827 0.120 7 20164512 intron variant A/C snv 0.27 6
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 6
rs12037879
LEPR
0.925 0.080 1 65477024 intron variant G/A;T snv 5
rs3923087
AXIN2
0.827 0.160 17 65553143 intron variant T/C snv 0.58 5
rs7336610
MIR17HG
0.827 0.240 13 91352883 intron variant C/T snv 0.47 5
rs9365723
SYNJ2
0.827 0.080 6 158014540 intron variant A/C;G snv 0.56 5
rs17026425
IQCM
0.882 0.080 4 149751362 intron variant G/A snv 4.9E-02 4
rs2075241
LRP6 ; BCL2L14
0.882 0.200 12 12138545 intron variant G/A;C snv 0.18 4
rs2470151
MIR7973-2 ; CYP19A1
0.925 0.080 15 51314872 intron variant C/T snv 0.29 4
rs2856838
IL1A
0.851 0.200 2 112782395 intron variant G/A snv 0.37 4
rs4998557
SOD1
0.851 0.080 21 31662579 intron variant G/A snv 0.22 4
rs6702619
LINC01708
0.851 0.200 1 99580690 intron variant T/G snv 0.35 4
rs932335
HSD11B1-AS1 ; HSD11B1
0.851 0.120 1 209732389 intron variant G/C snv 0.21 0.21 4
rs9620817
CHEK2
0.851 0.120 22 28712568 intron variant A/T snv 8.4E-02 4