Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs5743810
TLR6 ; TLR1
0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 21
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 17
rs1239681664
ABCA1
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs721917
SFTPD
0.752 0.360 10 79946568 missense variant A/G snv 0.47 0.42 14
rs5744174
TLR5
0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs6795970
SCN10A
0.807 0.200 3 38725184 missense variant A/G snv 0.65 0.70 13
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 9
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 9
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs3764147
LACC1
0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 7
rs7234029
PTPN2
0.807 0.320 18 12877061 intron variant A/G snv 0.27 7
rs13407913
ADCY3
0.827 0.120 2 24874775 intron variant A/G snv 0.54 6