Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs352142
TWF2
0.925 0.120 3 52232366 intron variant A/C snv 7.5E-02 2
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs1893352
TIRAP
1.000 0.080 11 126290792 intron variant A/C;G snv 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs5743810
TLR6 ; TLR1
0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 21
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs3764880
TLR8-AS1 ; TLR8
0.752 0.320 X 12906707 start lost A/G snv 0.31 0.30 11
rs10421768
HAMP
0.807 0.120 19 35281996 intron variant A/G snv 0.21 6
rs1978331
LTA4H
0.827 0.200 12 96015423 intron variant A/G snv 0.50 5
rs2280789
LOC105371744 ; CCL5
0.925 0.080 17 35879999 intron variant A/G snv 0.16 3
rs10499859
CD36
0.925 0.120 7 80629494 intron variant A/G snv 0.46 2
rs10841845
CLEC4E
0.925 0.200 12 8533837 3 prime UTR variant A/G snv 0.28 2
rs1135791
SP110
0.925 0.080 2 230177560 missense variant A/G snv 0.42 0.40 2
rs2367707
EREG
0.925 0.080 4 74382717 synonymous variant A/G snv 0.79 0.79 2
rs6853
MYD88
0.925 0.160 3 38142879 3 prime UTR variant A/G snv 0.16 2
rs10841847
CLEC4E
1.000 0.080 12 8535216 intron variant A/G snv 0.58 1