Disease: Behcet Syndrome
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs758548184
NOD2
0.851 0.240 16 50699557 missense variant G/C snv 5
rs9471535
TREM1
0.851 0.240 6 41287752 upstream gene variant T/C snv 0.12 5
rs10094579 0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18 6
rs1495965 0.790 0.280 1 67287825 intergenic variant C/T snv 0.55 8
rs2058660
IL18RAP
0.882 0.280 2 102437989 intron variant G/A snv 0.78 4
rs2838519
GATD3A
0.851 0.280 21 44195140 intron variant G/A;C snv 4
rs7234029
PTPN2
0.807 0.320 18 12877061 intron variant A/G snv 0.27 7
rs11230563
LOC105369326 ; CD6
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 8
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs762421
GATD3A
0.851 0.360 21 44195678 intron variant G/A snv 4
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs1343151
IL23R
0.752 0.400 1 67253446 intron variant G/A snv 0.41 10
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs2293152
STAT3
0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 10
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs2066844
NOD2
0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs696
NFKBIA
0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs17235409
SLC11A1
0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1884444
IL23R ; C1orf141
0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19