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
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 25
rs16910526
CLEC7A ; LOC105369655
0.742 0.280 12 10118488 stop gained A/C;G snv 6.2E-02 12
rs4077515
CARD9
0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41 11
rs41292470
LOC285626
0.925 0.200 5 159333192 intron variant TTAGAG/GC delins 3
rs775910328
TLR4
0.882 0.120 9 117713471 missense variant A/G snv 4.0E-06 3
rs1196547982
TLR2
0.925 0.120 4 153703650 missense variant A/G snv 4.0E-06 7.0E-06 2
rs748327912
CLEC7A ; LOC105369655
1.000 0.080 12 10125310 missense variant C/T snv 4.0E-06 1
rs8028958
SPTBN5
1.000 0.080 15 41863503 intron variant G/C;T snv 1