Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10911362
NCF2 ; SMG7
1.000 0.040 1 183579857 intron variant A/G snv 0.12 1
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs10956514
ASAP1
1.000 0.040 8 130240512 intron variant A/G snv 0.37 1
rs11012476
NEBL
0.925 0.120 10 21003994 intron variant C/T snv 3.5E-02 3
rs1101998
IFI16
1.000 0.040 1 159029494 intron variant C/T snv 0.65 1
rs11031728 1.000 0.040 11 32342070 intron variant C/G snv 0.18 1
rs11031731 0.925 0.040 11 32343884 upstream gene variant G/A snv 0.18 3
rs11040
TENT5A
1.000 0.040 6 81752132 missense variant C/A;G;T snv 1
rs11045819
SLCO1B1
0.851 0.120 12 21176879 missense variant C/A;T snv 0.11; 4.0E-06 4
rs11096957
TLR10
0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41 8
rs11117415
MIR6774 ; IRF8
1.000 0.040 16 85917080 intron variant A/G snv 0.12 1
rs11246213
IRF7
1.000 0.040 11 612967 intron variant A/G snv 0.25 0.33 1
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1131454
OAS1
0.882 0.040 12 112911065 missense variant G/A;C snv 0.57 3
rs1131498
C1orf112 ; SELL
0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs1135791
SP110
0.925 0.080 2 230177560 missense variant A/G snv 0.42 0.40 2
rs11466617
TLR10
1.000 0.040 4 38778850 intron variant T/C snv 0.13 2
rs11556887
SP110 ; SP140
1.000 0.040 2 230212961 missense variant G/A snv 0.10 7.4E-02 1
rs11567764
IL7R
1.000 0.040 5 35873503 missense variant G/A;T snv 9.5E-03; 4.0E-06 1
rs11575934
IL12RB1
0.882 0.040 19 18075808 missense variant T/C snv 0.28 0.25 4
rs11575935
IL12RB1
0.925 0.040 19 18063921 missense variant C/T snv 1.1E-02 5.7E-03 2
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22 13
rs11774633
ASAP1
1.000 0.040 8 130177997 intron variant C/T snv 0.61 1
rs1190662183
ICAM3
1.000 0.040 19 10338932 synonymous variant C/T snv 1
rs11958933
LINC02211
1.000 0.040 5 25323598 intron variant G/A snv 0.70 1