Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11216153
APOA1-AS
0.925 0.080 11 116834384 upstream gene variant G/T snv 0.16 2
rs1153879
STAG1
0.925 0.080 3 136392816 intron variant G/T snv 2
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs77874543
TNFRSF13C
0.882 0.080 22 41926712 missense variant G/C;T snv 6.1E-02 5.5E-02 3
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs11137480
S1PR3 ; C9orf47
0.882 0.120 9 88989662 upstream gene variant G/C snv 0.37 3
rs5744105
TLR5
0.925 0.080 1 223142735 intron variant G/C snv 0.57 2
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs2297630
CXCL12
0.827 0.160 10 44376100 intron variant G/A;T snv 0.21 6
rs17602729
AMPD1
0.925 0.080 1 114693436 stop gained G/A;T snv 8.6E-02 2
rs2715267
ILDR1
0.925 0.080 3 122052011 upstream gene variant G/A;T snv 2
rs945177
LOC105370124
1.000 0.080 13 27047848 intergenic variant G/A;T snv 1
rs2249825
HMGB1
0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs7096206
MBL2
0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs17281995
CD86
0.763 0.360 3 122120794 3 prime UTR variant G/A;C snv 11
rs4358188
BPI
0.827 0.160 20 38318446 missense variant G/A;C snv 0.46 7
rs2857656
CCL2
0.851 0.120 17 34254988 upstream gene variant G/A;C snv 5
rs5743867
TOLLIP
0.882 0.120 11 1307121 intron variant G/A;C snv 3
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78