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
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800972
DEFB1
0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
rs121918338
CARD9
0.807 0.160 9 136370362 stop gained G/A snv 1.2E-05 7.0E-06 7
rs121434254
AIRE
0.807 0.200 21 44289773 stop gained C/A;T snv 7.5E-04 6
rs398122363
CARD9
0.827 0.120 9 136370380 stop gained G/A snv 8.2E-06 7.0E-06 5
rs78645479
FOXD3-AS1 ; FOXD3
0.851 0.120 1 63322631 5 prime UTR variant C/G;T snv 4