Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 11
rs1015164
CCRL2
0.925 3 46410189 intron variant A/C;G;T snv 8
rs10808739
CYP7B1
0.882 8 64727703 intron variant G/A snv 0.24 6
rs143633948
ARG1
0.882 0.080 6 131504454 intron variant G/A;C snv 6
rs2442719
HLA-B
0.882 0.120 6 31352761 intron variant C/T snv 0.53 6
rs35897606
KIAA1549L
0.882 0.080 11 33436311 intron variant A/G snv 4.4E-02 6
rs73132848
CAV3 ; OXTR
0.882 0.080 3 8764738 intron variant G/A snv 9.3E-02 6
rs11649112
LOC107984137 ; SHISA9
0.925 16 13267554 intron variant G/A snv 0.22 5
rs12460243
FBN3
0.925 19 8066356 intron variant G/A snv 0.14 5
rs16823858 0.925 3 115559835 intron variant G/A;C snv 5
rs16933829
PIK3C2A
0.925 11 17094129 intron variant T/C snv 6.2E-02 5
rs17038463
CNTN6
0.925 3 1383484 intron variant T/C;G snv 5
rs17169
LINC00298 ; LINC00299
0.925 2 8037334 intron variant G/T snv 0.13 5
rs17691394
GRM8
0.925 7 126684537 intron variant A/G snv 0.13 5
rs3869068
ZNRD1ASP
0.925 6 30036275 intron variant C/T snv 0.17 5
rs59440261
MICA
0.925 6 31403294 intron variant C/A snv 3.3E-02 5
rs608114
LOC107986626
0.925 6 95928822 intron variant A/T snv 0.95 5
rs61550741
TIAM1
0.925 21 31133966 intron variant A/G snv 0.12 5
rs6542826
SH3RF3 ; RANBP2
0.925 2 109433263 intron variant A/G snv 0.51 5
rs1799937
WT1
0.882 0.160 11 32389228 intron variant A/G snv 0.35 0.35 3
rs2301254
WT1-AS ; WT1
0.882 0.160 11 32436129 intron variant A/G snv 0.48 3
rs2074560
MX2
0.925 0.040 21 41380411 intron variant A/G snv 0.43 2