Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 4
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 2
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 1
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 2
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 1
rs602662
LOC105447645 ; FUT2
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 1
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 1
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 1
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 2
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 3
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 1
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 1
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 1
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 2
rs33980500
TRAF3IP2-AS1 ; TRAF3IP2
0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 2
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 4
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3