Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs650108
MMP3
0.827 0.160 11 102838056 intron variant G/A snv 0.31 6
rs11747270
IRGM
0.790 0.240 5 150879305 intron variant A/G snv 0.21 7
rs2779249
NOS2
0.851 0.200 17 27801555 intron variant C/A snv 0.33 7
rs6596473
SLC23A1
0.807 0.120 5 139374887 intron variant G/C;T snv 7
rs1927907
TLR4
0.790 0.320 9 117710486 intron variant C/T snv 0.18 7
rs9533156
TNFSF11
0.807 0.280 13 42573535 intron variant T/C snv 0.47 8
rs2243248
IL4
0.763 0.240 5 132672952 upstream gene variant T/A;C;G snv 9
rs4612666
NLRP3
0.763 0.440 1 247435768 intron variant T/C snv 0.65 10
rs11225395
MMP8
0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs1800472
TGFB1
0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 11
rs7873784
TLR4
0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 11
rs11362
DEFB1
0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 13
rs396991
FCGR3A
0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs3811463
LIN28A
0.752 0.400 1 26427451 3 prime UTR variant T/A;C snv 14
rs652438
MMP12
0.716 0.400 11 102865911 missense variant T/C;G snv 7.1E-02; 2.5E-04 14
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs1050501
FCGR2B
0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs224222
MEFV
0.724 0.440 16 3254463 missense variant C/T snv 0.24 0.21 15
rs1800972
DEFB1
0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs6354
SLC6A4
0.732 0.280 17 30222880 5 prime UTR variant G/C;T snv 16
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs1800630
TNF ; LOC100287329 ; LTA
0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19