Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 6
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 5
rs1736135
LOC101927745
0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 4
rs2188962
IRF1-AS1
0.882 0.160 5 132435113 intron variant C/T snv 0.29 4
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 4
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs864745
JAZF1
0.763 0.320 7 28140937 intron variant T/C snv 0.41 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 3
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs11747270
IRGM
0.790 0.240 5 150879305 intron variant A/G snv 0.21 3
rs1250550
ZMIZ1
0.851 0.240 10 79300560 intron variant C/A snv 0.27 3
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 3
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45 3
rs1551398
LOC105375746
0.882 0.160 8 125527809 intron variant G/A snv 0.48 3