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
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 17
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs2695121
NR1H2
0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 16
rs1239681664
ABCA1
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs1861494
IFNG-AS1 ; IFNG
0.716 0.400 12 68157629 intron variant C/T snv 0.75 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
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11