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
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs17235409
SLC11A1
0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs10877012
CYP27B1 ; METTL1
0.763 0.280 12 57768302 intron variant G/C;T snv 10
rs1800076
CFTR
0.763 0.200 7 117509093 missense variant G/A;T snv 1.5E-02; 8.0E-06 10
rs9298814
IFNA17
0.790 0.160 9 21227623 missense variant A/C;G snv 0.12; 8.8E-06 7
rs10399931
CHI3L1
0.807 0.320 1 203186952 upstream gene variant T/A;C snv 6
rs615672
HLA-DRB1
0.851 0.240 6 32606394 intergenic variant G/A;C snv 6
rs10213865
LOC105374724 ; IL7R
0.827 0.120 5 35857748 intron variant A/C;T snv 5
rs2239804
HLA-DRA
0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 5
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs1049550
ANXA11
0.882 0.160 10 80166946 missense variant G/A;C snv 0.42; 4.2E-06 4
rs2239802
HLA-DRA
0.882 0.200 6 32444069 intron variant C/A;G;T snv 4
rs2523589 0.851 0.200 6 31359557 upstream gene variant G/A;T snv 4
rs4988453
MYD88 ; ACAA1
0.851 0.200 3 38137763 upstream gene variant C/A;T snv 4
rs9378212 0.925 0.160 6 32477914 upstream gene variant C/G;T snv 4
rs28366298
HLA-DRB1
0.925 0.120 6 32593082 upstream gene variant A/C;T snv 3
rs412657 0.882 0.240 6 32243308 intergenic variant T/C;G snv 3
rs5020946 0.925 0.160 6 32482312 intergenic variant G/C;T snv 3