Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 11
rs769449
APOE
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 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
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 10
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 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
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 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
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 8
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs643434
ABO
9 133266942 intron variant A/G;T snv 8