Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5743867
TOLLIP
0.882 0.120 11 1307121 intron variant G/A;C snv 3
rs6958571
NOD1
0.925 0.080 7 30446094 intron variant A/C;G snv 1.2E-05; 0.25; 5.3E-05 3
rs805305
DDAH2
0.882 0.120 6 31729610 intron variant C/G snv 0.48 3
rs1153879
STAG1
0.925 0.080 3 136392816 intron variant G/T snv 2
rs11666254
FPR2 ; FPR1
0.925 0.080 19 51759909 intron variant A/G snv 0.28 2
rs2332096
CD86
0.925 0.080 3 122102296 intron variant T/A;G snv 2
rs2808530
GABBR2
0.925 0.080 9 98576823 intron variant A/C snv 0.12 2
rs4755453
TRAF6 ; RAG1
0.925 0.080 11 36509094 intron variant C/A;G;T snv 2
rs5744105
TLR5
0.925 0.080 1 223142735 intron variant G/C snv 0.57 2
rs595209
TIRAP
0.925 0.080 11 126292326 intron variant A/C;G snv 2
rs150062338
LPP
1.000 0.080 3 188287160 intron variant C/T snv 3.6E-02 1
rs58764888
HRH1
1.000 0.080 3 11176005 intron variant T/A snv 5.8E-02 1
rs945177
LOC105370124
1.000 0.080 13 27047848 intergenic variant G/A;T snv 1
rs17602729
AMPD1
0.925 0.080 1 114693436 stop gained G/A;T snv 8.6E-02 2
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78