Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 8
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 8
rs643434
ABO
9 133266942 intron variant A/G;T snv 7
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 7
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 6
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs11508026
CETP
16 56965416 intron variant C/T snv 0.32 5
rs814295
GCKR
0.925 0.120 2 27520348 intron variant A/G snv 0.18 5
rs9268858
HLA-DRB9
0.882 0.200 6 32461981 intron variant T/C snv 0.29 5
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 5
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 5
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 5
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 4
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 4
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 4
rs769449
APOE
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 4
rs13233571
BCL7B
0.925 0.120 7 73556901 intron variant C/T snv 9.2E-02 4
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 4