Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs17235409
SLC11A1
0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs1518111
IL19 ; IL10
0.790 0.360 1 206771300 intron variant T/C snv 0.71 9
rs2234671
CXCR1
0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11 7
rs3024498
IL10
0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20 7
rs1554286
IL19 ; IL10
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72 7
rs79071878
LOC105379176 ; IL4
0.827 0.240 5 132680652 intron variant ATGAAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGACGATGGTGGCGTGGACAGAATGAAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGATGATGGTGGCGTGGACAGAAT/- del 7
rs17235416
SLC11A1
0.807 0.200 2 218395091 3 prime UTR variant TGTG/- del 8.4E-02 6
rs17221959
SLC11A1
0.882 0.160 2 218387907 synonymous variant C/T snv 7.0E-02 0.12 3
rs2276631
SLC11A1
0.882 0.120 2 218384290 missense variant C/T snv 0.23 0.23 3
rs2279015
SLC11A1
0.882 0.080 2 218394547 non coding transcript exon variant G/A snv 0.51 3
rs9271858 1.000 0.040 6 32627446 upstream gene variant A/G snv 0.44 1
rs3138060
CXCR1
1.000 0.040 2 218166777 intron variant G/C snv 7.1E-02 1
rs4674259
CXCR2
1.000 0.040 2 218126282 5 prime UTR variant G/A;T snv 1
rs2103816
FAM120B
1.000 0.040 6 170366925 intron variant T/A snv 0.58 1
rs17549193
FCN2
1.000 0.040 9 134887180 missense variant C/T snv 0.26 0.30 1
rs754692430
IL2RB
1.000 0.040 22 37135413 missense variant C/G;T snv 1.2E-05; 8.0E-06 1
rs9460106
LOC112267971 ; FAM120B
1.000 0.040 6 170306872 intron variant T/C;G snv 1