Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 15
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 13
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 11
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 10
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 9
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 9
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 9