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
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs7529229
IL6R
0.851 0.120 1 154448302 intron variant T/C snv 0.48 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
rs2129979 1.000 0.080 4 110799841 downstream gene variant T/G snv 0.39 1
rs223888
CCL22
1.000 0.080 16 57357856 upstream gene variant A/G;T snv 1