Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs5744168
TLR5
0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs5743551
TLR1
0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs7194886 0.851 0.080 16 50691282 upstream gene variant C/T snv 0.38 4
rs76600635
TLR1
0.925 0.040 4 38798702 missense variant A/G snv 8.2E-03 2.8E-03 3
rs138968705
TLR6 ; TLR1
0.925 0.080 4 38828278 missense variant G/A snv 1.2E-04 2.3E-04 2
rs6757121
SLC30A6 ; NLRC4
1.000 0.040 2 32224192 3 prime UTR variant C/T snv 9.7E-02 1
rs376729946
TLR6 ; TLR1
1.000 0.040 4 38828732 missense variant C/T snv 1.2E-05 4.9E-05 1