Source: BEFREE

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-06 221
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs1927914
TLR4
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52 14
rs7873784
TLR4
0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 11
rs5030717
TLR4
0.807 0.240 9 117711556 intron variant A/G snv 0.13 9
rs5030718
TLR4
0.827 0.200 9 117713548 stop gained G/A;T snv 3.1E-03; 8.0E-06 8
rs1191926239
TLR4
0.807 0.200 9 117704539 missense variant C/G snv 4.0E-06 7
rs754342091
TLR4
0.790 0.200 9 117712421 missense variant A/G snv 3.2E-05 1.4E-05 7
rs1927907
TLR4
0.790 0.320 9 117710486 intron variant C/T snv 0.18 7
rs5030728
TLR4
0.807 0.160 9 117712004 intron variant G/A;T snv 0.23 7
rs11536878
TLR4
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02 5
rs12377632
TLR4
0.827 0.120 9 117710452 intron variant T/A;C snv 5
rs1057317
TLR4
0.827 0.160 9 117715764 3 prime UTR variant C/A snv 5
rs1179225338
TLR4
0.851 0.120 9 117713505 synonymous variant C/T snv 4.0E-06 4
rs11536891
TLR4
0.851 0.120 9 117717059 3 prime UTR variant T/C snv 0.16 4
rs775910328
TLR4
0.882 0.120 9 117713471 missense variant A/G snv 4.0E-06 3
rs11536898
TLR4
0.882 0.080 9 117717932 3 prime UTR variant C/A snv 0.14 3
rs1554973
TLR4
0.882 0.120 9 117718534 3 prime UTR variant T/C snv 0.38 3
rs7037117
TLR4
0.882 0.040 9 117721385 3 prime UTR variant A/G snv 0.40 3
rs1374607932
TLR4
0.882 0.280 9 117713653 missense variant G/A snv 7.0E-06 3
rs200527106
TLR4
0.925 0.120 9 117712902 missense variant G/A;C snv 4.0E-06 3