Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 7
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 7
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 5
rs2249742
HLA-B ; HLA-C
0.925 0.120 6 31272944 intron variant C/T snv 0.50 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
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 5
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 5
rs2227139 0.925 0.160 6 32445682 downstream gene variant G/A snv 0.61 4
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 4
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs9402686
LOC105378010
6 135106679 upstream gene variant G/A snv 0.20 4
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 4
rs3094212
PSORS1C1 ; CDSN
1.000 6 31117993 non coding transcript exon variant G/A snv 0.58 4
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 3
rs4794822 17 40000459 downstream gene variant C/G;T snv 3
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 3