Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1324694
ERLIN1
0.925 0.120 10 100186688 upstream gene variant C/T snv 7.8E-02 2
rs3917010
VCAM1
1.000 0.080 1 100725310 intron variant A/C snv 0.18 1
rs2227631
SERPINE1
0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs769665945
SERPINE1
0.882 0.160 7 101137079 missense variant C/A;T snv 4.0E-06; 3.6E-05 3
rs12316150
OLR1
1.000 0.080 12 10159692 3 prime UTR variant A/T snv 7.4E-02 1
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs6218
LINC02456 ; HELLPAR ; IGF1
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs978458
IGF1 ; LINC02456
0.925 0.120 12 102408461 intron variant T/C snv 0.69 2
rs2072592
IGF1 ; LINC02456
0.925 0.120 12 102419854 intron variant C/T snv 2.8E-02 2
rs7956547
IGF1
0.925 0.120 12 102465038 intron variant T/C snv 0.25 2
rs2162679
IGF1
0.851 0.240 12 102477481 intron variant C/G;T snv 6
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs635746
WTAPP1
1.000 0.080 11 102832897 non coding transcript exon variant A/G snv 0.54 1
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs569444
WTAPP1 ; MMP3
0.925 0.120 11 102836574 non coding transcript exon variant G/A;T snv 0.12; 6.7E-06 0.10 3
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs572527200
MMP12
0.882 0.240 11 102875064 upstream gene variant T/C snv 4
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs2019090 1.000 0.080 11 103798234 intron variant A/C;G;T snv 1
rs539179964
RIMS2
0.882 0.080 8 104248720 missense variant C/T snv 1.6E-05 4.2E-05 3
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs2230808
ABCA1
0.827 0.240 9 104800523 missense variant T/C snv 0.71 0.60 6