Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 4
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 4
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs7518199
IL6R
1 154434943 intron variant A/C;T snv 0.39; 4.2E-06 4
rs7529229
IL6R
0.851 0.120 1 154448302 intron variant T/C snv 0.48 4
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 4
rs3758348
SURF4
9 133372523 intron variant G/C snv 0.13 4
rs12967135 18 60181790 intergenic variant G/A snv 0.24 3
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 3
rs13244268
BAZ1B
0.925 0.120 7 73497513 intron variant T/C snv 9.2E-02 3
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 3
rs3027012
CADM3-AS1 ; ACKR1
1 159204333 5 prime UTR variant C/T snv 0.13 3
rs3817588
GCKR
0.882 0.160 2 27508345 intron variant T/C snv 0.14 3
rs2259816
HNF1A
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 3
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 3
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 3
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 3
rs10512597
RAB37 ; CD300LF
17 74703694 intron variant T/A;C snv 3
rs10119
TOMM40
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 3
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 3
rs10908713 1 159369769 intron variant T/C snv 0.47 2
rs11265174 1 159350569 intron variant T/A snv 0.35 2
rs11265196 1 159448422 intron variant G/A snv 0.47 2
rs12034864 1 159215190 regulatory region variant A/C;G;T snv 2
rs12047230 1 159509215 intergenic variant A/G snv 0.33 2