Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 15
rs1256046734
LEPR
0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 11
rs9461776
HLA-DRB1
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs2308327
MGMT
0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02 10
rs1049216
CASP3
0.790 0.200 4 184628935 3 prime UTR variant A/G snv 0.27 9
rs2305160
NPAS2 ; NPAS2-AS1
0.776 0.200 2 100974842 missense variant A/G snv 0.71 0.75 9
rs2072633
CFB ; CYP21A2 ; NELFE
0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59 6
rs2844484
LTA ; LOC100287329
0.807 0.320 6 31568447 upstream gene variant A/G snv 0.64 6
rs2069812
IL5
0.851 0.240 5 132544224 intron variant A/G snv 0.54 5
rs537160
CYP21A2 ; CFB
0.882 0.240 6 31948623 intron variant A/G snv 0.73 4
rs11038689
CRY2
0.882 0.160 11 45852713 intron variant A/G snv 0.19 3
rs3900115
CASP10
1.000 0.120 2 201185954 synonymous variant A/G snv 0.45 0.49 3
rs8094402
MBP
0.882 0.120 18 76995493 intron variant A/G snv 0.25 3
rs3789068
MIR4435-2HG ; BCL2L11
0.925 0.120 2 111151670 intron variant A/G snv 0.41 2
rs1185926926
SLC19A1
1.000 0.120 21 45531748 missense variant A/G snv 4.1E-06 1
rs13178127
XRCC4
1.000 0.120 5 83293613 intron variant A/G snv 3.3E-02 1
rs1320767909
SLC19A1
1.000 0.120 21 45531982 missense variant A/G snv 4.1E-06 1
rs1335035506
SHMT1
1.000 0.120 17 18340207 missense variant A/G snv 4.0E-06 1.4E-05 1
rs1921310
TANK
1.000 0.120 2 161192690 intron variant A/G snv 0.15 1
rs2991216
SYK
1.000 0.120 9 90865745 intron variant A/G snv 0.21 1
rs754651345
IL12B ; LOC107986469
1.000 0.120 5 159326751 missense variant A/G snv 4.0E-06 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs872071
IRF4
0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 13