Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs2267437
DESI1 ; XRCC6
0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 18
rs5751129
XRCC6 ; DESI1
0.752 0.320 22 41619761 intron variant C/T snv 0.69 14
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs132774
XRCC6
0.776 0.280 22 41635949 intron variant C/G snv 0.69 9
rs6713088
ACYP2
0.763 0.200 2 54118332 intron variant C/G snv 0.48 9
rs843711
ACYP2
0.790 0.200 2 54251980 intron variant C/T snv 0.41 7
rs9420907
STN1
0.790 0.320 10 103916707 intron variant C/A;G snv 7
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 6
rs7859384 0.882 0.120 9 79507370 intron variant A/C;G snv 6
rs3783546
IL1A
0.882 0.160 2 112777253 intron variant G/C snv 0.70 5
rs3783550
IL1A
0.827 0.200 2 112775308 intron variant G/T snv 0.64 0.70 5
rs390802
DNAH1
0.827 0.160 3 52397655 intron variant G/A snv 0.16 5