Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17008504 1.000 0.160 4 124718662 intergenic variant T/A snv 4.3E-02 1
rs2271100
AGA
1.000 0.160 4 177438525 intron variant T/C snv 0.19 1
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 7
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
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs2397084
IL17F
0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 7
rs7773456 0.925 0.160 6 19823007 intron variant T/G snv 0.35 2
rs114580964
PRRC2A
1.000 0.160 6 31636736 missense variant C/A;T snv 3.4E-03 1.4E-03 1
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs1456896 0.882 0.200 7 50264865 upstream gene variant C/T snv 0.67 5
rs11981433
PON2
0.882 0.240 7 95425028 intron variant T/C;G snv 4
rs7834765
LOC107986971
0.925 0.160 8 121263666 regulatory region variant G/T snv 0.32 2
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs601162 0.925 0.160 9 29632144 upstream gene variant A/C;G;T snv 2
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs2295415
CREM
0.882 0.160 10 35212510 3 prime UTR variant A/G snv 0.19 3
rs1108131
CAMK1D
0.925 0.160 10 12455748 intron variant T/C snv 0.28 2