Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs45487298
HSD11B1-AS1 ; HSD11B1
0.882 0.120 1 209706871 intron variant -/A delins 3
rs1799768
SERPINE1
0.807 0.360 7 101126425 upstream gene variant -/A;C ins 6
rs146052672
HMGA1
0.851 0.160 6 34242693 intron variant -/C delins 5
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs712
KRAS
0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 4
rs12988520
UGT1A6 ; UGT1A9 ; UGT1A8 ; UGT1A10 ; UGT1A7
1.000 0.040 2 233698748 intron variant A/C snv 0.51 3
rs164147
NOS1AP
0.882 0.080 1 162368607 3 prime UTR variant A/C snv 0.76 3
rs1797912
PPARG
1.000 0.040 3 12428740 intron variant A/C snv 0.33 3
rs8179252
GCKR
0.882 0.120 2 27523965 downstream gene variant A/C snv 0.37 3
rs3017887
NOX4
0.925 0.120 11 89492920 intron variant A/C snv 0.81 2
rs295
LPL
1.000 0.040 8 19958727 intron variant A/C snv 0.28 1
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs1997623
CAV1
0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 9
rs561005732
GGT1
0.925 0.040 22 24627519 missense variant A/C;G snv 8.0E-06 2
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 4
rs1441756 1.000 0.040 8 20010875 intergenic variant A/C;G;T snv 1
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 10
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 7
rs180349 0.925 0.200 11 116741111 intergenic variant A/C;T snv 5