Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
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
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 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
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 3
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 3
rs3027012
CADM3-AS1 ; ACKR1
1 159204333 5 prime UTR variant C/T snv 0.13 3
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 3
rs10908713 1 159369769 intron variant T/C snv 0.47 2
rs11265174 1 159350569 intron variant T/A snv 0.35 2
rs11265190
OR10J1
1 159421611 intron variant G/A snv 0.47 2
rs11265196 1 159448422 intron variant G/A snv 0.47 2
rs12034383
CR1
1 207630250 intron variant G/A snv 0.47 2
rs12034864 1 159215190 regulatory region variant A/C;G;T snv 2
rs12034969
OR10J1
1 159415154 intron variant T/C snv 0.46 2
rs12047230 1 159509215 intergenic variant A/G snv 0.33 2
rs12072644 1 159245497 intergenic variant C/A;T snv 2
rs12739022 1 159689641 intergenic variant T/C snv 0.24 2
rs12741825 1 159700355 downstream gene variant C/T snv 0.24 2
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 2
rs12754915 1 159691079 intergenic variant T/C snv 0.25 2