Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1400094618
MOK
0.882 0.240 14 102229508 missense variant A/G snv 3
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs782656324
CUX1
0.925 0.120 7 102273394 missense variant C/G;T snv 8.1E-06 2
rs2548724
SLCO4C1
1.000 0.080 5 102284470 intron variant T/C snv 0.81 1
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs6218
LINC02456 ; HELLPAR ; IGF1
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 12
rs5742632
LINC02456 ; IGF1
0.851 0.120 12 102462696 intron variant A/G snv 0.26 4
rs5742612
LOC105369944 ; IGF1
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02 11
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs363050
SNAP25-AS1 ; SNAP25
0.790 0.240 20 10253609 intron variant G/A snv 0.57 8
rs768698948
NFKB1
1.000 0.080 4 102579012 missense variant G/A;T snv 8.0E-06 1
rs7667496
NFKB1
1.000 0.080 4 102588298 intron variant C/G;T snv 1
rs2540317
MFSD9
1.000 0.080 2 102733348 intron variant A/G;T snv 1
rs4729854
RASA4DP
1.000 0.080 7 102743216 intron variant T/A snv 0.35 1
rs7729395
PAM
1.000 0.080 5 102764872 intron variant C/T snv 3.1E-02 2
rs16869786 1.000 0.080 8 102777227 regulatory region variant T/C snv 1.4E-02 1
rs12147254
TRAF3
0.851 0.240 14 102799329 intron variant G/A snv 0.23 4
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs17115149
CYP17A1
0.882 0.160 10 102837961 upstream gene variant G/A;T snv 4
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs12435483
TRAF3
1.000 0.080 14 102865271 intron variant C/T snv 0.14 2
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13