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
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
rs2269426
TNXB
0.807 0.280 6 32108722 intron variant G/A snv 0.35 8
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 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
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 6
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 6
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs3131379
MSH5 ; MSH5-SAPCD1
0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 6
rs558702
C2 ; ZBTB12 ; CYP21A2
0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 5
rs2239804
HLA-DRA
0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 5
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs3130564
PSORS1C1
0.790 0.360 6 31133897 intron variant C/T snv 0.14 5
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv 5
rs5754217
UBE2L3
0.925 0.120 22 21585386 intron variant G/T snv 0.31 5
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 5
rs805303
BAG6
0.925 0.160 6 31648589 intron variant G/A snv 0.45 5
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4