Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs16147
LOC107986777 ; NPY
0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs2066847
NOD2
0.716 0.400 16 50729868 frameshift variant C/-;CC delins 1.5E-02 18
rs2276109
MMP12
0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 18
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs3819024
IL17A
0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs4711998
IL17A
0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50 15
rs1861494
IFNG-AS1 ; IFNG
0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs2670660
NLRP1
0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs72661131
MBL2
0.742 0.480 10 52771739 upstream gene variant A/G snv 7.6E-04 15
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs1927914
TLR4
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52 14
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs2146323
VEGFA
0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 13