Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 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
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 4
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 3
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 3
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 3
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 3
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 3
rs657555
PTPN2
0.925 0.080 18 12847137 intron variant C/A;T snv 3
rs762421
GATD3A
0.851 0.360 21 44195678 intron variant G/A snv 3
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 3
rs10114470
TNFSF15
0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 2
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 2
rs11742570 0.925 0.040 5 40410482 upstream gene variant T/C;G snv 2
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 2