Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15
rs749140677
VDR
0.752 0.240 12 47857185 missense variant G/A snv 8.0E-06 13
rs1898830
TLR2
0.807 0.280 4 153687301 intron variant A/G snv 0.30 10
rs11003123
MBL2
0.827 0.200 10 52771774 upstream gene variant G/A snv 0.30 6
rs1554973
TLR4
0.882 0.120 9 117718534 3 prime UTR variant T/C snv 0.38 3
rs1634323
TLR7
0.882 0.200 X 12870008 intron variant A/G snv 0.11 3
rs36014597
MBL2
1.000 0.080 10 52772040 upstream gene variant T/C snv 0.30 2
rs6517158
IL10RB
1.000 0.080 21 33299436 intron variant T/C;G snv 1
rs2231947
NODAL
1.000 0.080 10 70434098 intron variant G/A snv 0.18 1
rs5743737
TLR7
1.000 0.080 X 12872902 intron variant A/G snv 2.6E-02 1