Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 8
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs2894207
LINC02571 ; HLA-B
0.882 0.160 6 31295974 intron variant T/C snv 0.20 6
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs12191877
HLA-B
0.851 0.120 6 31285148 intron variant C/T snv 0.12 5
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 5
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 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
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 3
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 3
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 3
rs3134792
HLA-B
0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 3
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 3
rs657555
PTPN2
0.925 0.080 18 12847137 intron variant C/A;T snv 3
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 3
rs702873
LINC01185
0.882 0.120 2 60854407 intron variant C/T snv 0.35 3
rs10782001
FBXL19
1.000 0.040 16 30931304 intron variant G/A snv 0.53 2
rs10852936
ZPBP2
0.925 0.120 17 39875461 intron variant C/T snv 0.39 0.40 2