Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv 15
rs3087456
CIITA ; LOC105371080
0.742 0.480 16 10877045 intron variant G/A snv 0.53 14
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13 10
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs3131379
MSH5 ; MSH5-SAPCD1
0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 10
rs3130564
PSORS1C1
0.790 0.360 6 31133897 intron variant C/T snv 0.14 7
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 7
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 6
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv 6
rs558702
C2 ; ZBTB12 ; CYP21A2
0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs3129939
TSBP1-AS1 ; TSBP1
0.827 0.360 6 32368989 intron variant A/G snv 0.14 5
rs204990
GPSM3
0.851 0.280 6 32193653 intron variant C/A;T snv 4
rs4574025
TNFRSF11A
0.882 0.160 18 62342581 intron variant C/T snv 0.55 4
rs1265159
POU5F1
0.882 0.240 6 31172270 intron variant G/A snv 0.21 3
rs2893321
TNFSF13B
0.882 0.200 13 108290686 intron variant A/G snv 0.20 3
rs3792783
TNIP1
0.882 0.280 5 151076171 intron variant A/G snv 0.25 3
rs1422673
TNIP1
0.925 0.160 5 151059427 intron variant C/G;T snv 2
rs2071591
ATP6V1G2-DDX39B ; ATP6V1G2 ; NFKBIL1
0.925 0.160 6 31548022 intron variant G/A;C snv 2
rs2233287
TNIP1
0.925 0.160 5 151060536 intron variant G/A snv 0.11 2