Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 8
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 8
rs2269426
TNXB
0.807 0.280 6 32108722 intron variant G/A snv 0.35 8
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 8
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs12663103
GPSM3
0.851 0.240 6 32193547 intron variant T/C snv 6.1E-02 7
rs2516509
MICB-DT
0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs2523535 0.851 0.200 6 31368473 intron variant A/G snv 0.32 7
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs6457374
HLA-B ; LOC112267902
0.851 0.200 6 31304484 intron variant C/T snv 0.81 7
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13 6