Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8064821
SOCS3 ; LOC101928674
0.851 0.120 17 78361310 intron variant C/A snv 0.17 6
rs10490571
IL1R1
0.827 0.320 2 102100877 intron variant C/T snv 0.29 5
rs56061981
CXCL10 ; ART3
0.851 0.120 4 76023632 intron variant C/T snv 7.6E-02 5
rs2723176
IL37
0.851 0.200 2 112914932 intron variant A/C;G snv 4
rs3794624
CYBA
0.882 0.120 16 88650666 intron variant G/A snv 0.26 0.29 4
rs3800229
FOXO3
1.000 0.040 6 108675760 intron variant G/T snv 0.54 4
rs4842407 0.882 0.200 12 78807293 intron variant A/G snv 0.35 4
rs11012476
NEBL
0.925 0.120 10 21003994 intron variant C/T snv 3.5E-02 3
rs12998782
MARCO
0.882 0.160 2 118967804 intron variant C/T snv 0.19 3
rs1405655
NR1H2
0.925 0.120 19 50379362 intron variant T/C;G snv 3
rs2071277
NOTCH4
0.882 0.200 6 32203906 intron variant T/C snv 0.48 0.46 3
rs2243268
IL4
0.882 0.040 5 132678271 intron variant A/C snv 0.23 3
rs2243274
IL4 ; LOC105379176
0.882 0.080 5 132679140 intron variant G/A snv 0.34 3
rs2280789
LOC105371744 ; CCL5
0.925 0.080 17 35879999 intron variant A/G snv 0.16 3
rs3755276
IL18R1
0.925 0.120 2 102361999 intron variant C/T snv 0.45 3
rs5743604
TLR1
0.925 0.040 4 38799664 intron variant A/G snv 0.36 3
rs10500804
CYP2R1
0.925 0.040 11 14888727 intron variant T/G snv 0.35 2
rs11466617
TLR10
1.000 0.040 4 38778850 intron variant T/C snv 0.13 2
rs160441 1.000 0.040 8 89644760 intron variant T/C snv 0.55 2
rs17722851
NOS2
0.925 0.040 17 27783810 intron variant T/A snv 9.9E-02 2
rs1974675
IL18R1
1.000 0.040 2 102369915 intron variant G/A snv 0.45 2
rs206016
NOTCH4
0.925 0.160 6 32213405 intron variant G/A snv 0.14 2
rs2071285
NOTCH4
0.925 0.160 6 32212654 intron variant A/T snv 7.0E-02 5.4E-02 2
rs218916 1.000 0.040 8 89688709 intron variant C/T snv 0.67 2
rs2723186
IL37
0.925 0.160 2 112917503 intron variant A/G;T snv 0.91 2