Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs61752717
MEFV
0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs2066844
NOD2
0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs8177374
TIRAP
0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs2066842
NOD2
0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 15
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs2856836
IL1A
0.763 0.280 2 112774506 3 prime UTR variant A/G snv 0.26 9
rs774359492
WDHD1
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06 7
rs27044
ERAP1 ; LOC102724748
0.827 0.240 5 96783148 missense variant G/C snv 0.69 0.71 5
rs10050860
ERAP1
0.882 0.240 5 96786506 missense variant C/T snv 0.15 0.16 4
rs17482078
LOC102724748 ; ERAP1
0.882 0.240 5 96783162 missense variant C/G;T snv 2.8E-05; 0.15 4
rs41494349
LRP5
0.882 0.080 11 68348021 missense variant A/G snv 1.9E-02 8.2E-03 4
rs1894399
IL1A
0.925 0.040 2 112782600 intron variant C/T snv 0.32 2
rs3811058
IL1F10
0.925 0.040 2 113074368 missense variant T/A;C snv 4.0E-06; 0.13 2
rs3181357
DELEC1 ; TNFSF8
1.000 0.040 9 114930064 intron variant G/A;T snv 0.13; 5.3E-05 1
rs7761118
MAPK14
1.000 0.040 6 36100526 intron variant G/A snv 0.14 1