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
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
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs2854744
IGFBP3
0.695 0.520 7 45921476 intron variant G/T snv 0.48 20
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
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv 15
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
rs12921862
AXIN1
0.763 0.200 16 331927 intron variant C/A snv 0.18 10
rs132774
XRCC6
0.776 0.280 22 41635949 intron variant C/G snv 0.69 9
rs9582036
FLT1
0.776 0.280 13 28311271 intron variant C/A snv 0.59 8
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
rs3774262
ADIPOQ ; ADIPOQ-AS1
0.851 0.200 3 186854025 intron variant G/A snv 0.10 5