Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs9270986
HLA-DRB1
0.882 0.160 6 32606283 intergenic variant A/C snv 0.85 3
rs1805010
IL4R
0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 12
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 11
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 10
rs9277534
HLA-DPB1
0.790 0.280 6 33087030 3 prime UTR variant A/G snv 0.38 7
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 6
rs3129939
TSBP1-AS1 ; TSBP1
0.827 0.360 6 32368989 intron variant A/G snv 0.14 5
rs3129963 0.851 0.280 6 32412431 downstream gene variant A/G snv 0.17 4
rs1634718
MUC22
0.925 0.160 6 31005088 regulatory region variant A/G snv 0.20 3
rs2844657 0.882 0.240 6 30861745 upstream gene variant A/G snv 0.17 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
rs17209237
NR3C1
1.000 0.120 5 143277647 downstream gene variant A/G snv 0.18 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 13
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 10
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 7
rs204990
GPSM3
0.851 0.280 6 32193653 intron variant C/A;T snv 4