Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 1
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 7
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 6
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 5
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 2
rs12083537
IL6R
0.882 0.200 1 154408627 intron variant A/G snv 0.22 1
rs1805096
LEPR
0.827 0.200 1 65636574 synonymous variant G/A snv 0.46 0.43 1
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 8
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 6
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 5
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 4
rs7953249
HNF1A-AS1
0.882 0.160 12 120965921 splice region variant G/A snv 0.59 4
rs3817588
GCKR
0.882 0.160 2 27508345 intron variant T/C snv 0.14 3
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 3
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 3
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 2
rs2524163
HLA-B
0.925 0.160 6 31291802 intron variant C/T snv 0.66 2
rs7305618
HNF1A-AS1
0.925 0.160 12 120965129 intron variant C/T snv 0.28 2
rs9378212 0.925 0.160 6 32477914 upstream gene variant C/G;T snv 2
rs1834481
IL18
0.882 0.160 11 112153104 non coding transcript exon variant C/G snv 0.16 1
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 1