Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs1899663
HOTAIR
0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs1412125
HMGB1
0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1535045
CD40
0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs4513061
AGBL1
0.807 0.080 15 86428401 intron variant G/A;T snv 6
rs3124599
NOTCH1
0.851 0.080 9 136509318 intron variant G/A snv 0.13 5
rs36600
MTMR3
0.827 0.080 22 29941597 intron variant T/C snv 0.78 5
rs3787728
LOC100133286 ; CBR1 ; SETD4
0.851 0.080 21 36071595 intron variant T/C snv 0.74 5
rs6790167
TP63
0.827 0.080 3 189869485 intron variant A/G snv 0.53 5
rs116427960
HLA-B
0.925 0.120 6 31351449 intron variant C/G;T snv 3
rs942190
TDP1 ; EFCAB11
1.000 0.080 14 89956320 intron variant T/C snv 0.37 2
rs10118776
LOC107987046 ; IL33
1.000 0.080 9 6227418 intron variant G/A snv 0.94 1
rs12200782
BTN3A1
1.000 0.080 6 26402808 intron variant C/G snv 7.9E-02 1
rs140013431
BMP6
1.000 0.080 6 7770278 intron variant T/C snv 1.2E-02 1
rs17185553
ADAMTSL1
1.000 0.080 9 17934122 intron variant G/C snv 6.5E-02 1
rs1778335
PIP4K2A
1.000 0.080 10 22643219 intron variant T/C snv 0.27 1
rs3134425
CRTAM
1.000 0.080 11 122838470 intron variant T/C snv 0.67 1
rs7519667
WDR64
1.000 0.080 1 241722005 intron variant C/T snv 0.78 1
rs8049634
LOC654780 ; ADAD2
1.000 0.080 16 84192073 intron variant A/G snv 0.35 1
rs9308062
TMA16
1.000 0.080 4 163517048 intron variant T/A;C snv 1
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs141670911 1.000 0.080 6 26581030 intergenic variant A/T snv 7.3E-02 1