Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800057
ATM
0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 11
rs611646
ATM
0.882 0.120 11 108306370 intron variant T/A;C snv 3
rs74911261
POGLUT3
0.882 0.160 11 108486410 missense variant G/A snv 1.6E-02 1.6E-02 4
rs1416313401
SYBU
0.827 0.160 8 109578004 missense variant A/G snv 4.1E-06 5
rs7483
GSTM3 ; GSTM5
0.742 0.320 1 109737079 missense variant C/T snv 4.0E-06; 0.35 0.26 11
rs1332018
GSTM5 ; GSTM3
0.882 0.200 1 109740350 5 prime UTR variant G/T snv 0.64 0.66 6
rs333951
CSF1
0.925 0.120 1 109909068 upstream gene variant T/C snv 0.74 2
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs2050462
CSF1
0.925 0.120 1 109930334 3 prime UTR variant T/A;G snv 2
rs1057519915
MTOR
0.851 0.160 1 11109318 missense variant A/C snv 5
rs1057519916
MTOR
0.882 0.160 1 11109320 missense variant T/A snv 4
rs587777894
MTOR
0.776 0.240 1 11124516 missense variant G/A;T snv 9
rs1057519917
MTOR
0.807 0.160 1 11124517 missense variant A/G;T snv 7
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1057519913
MTOR
0.925 0.120 1 11157172 missense variant G/C snv 3
rs786205165
MTOR
0.882 0.120 1 11157173 missense variant C/A;T snv 4
rs1057519914
MTOR
0.851 0.240 1 11157174 missense variant A/G snv 5
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs1982809
BTLA ; LOC112268446
0.882 0.200 3 112463893 downstream gene variant A/G snv 0.28 3
rs2295080
MTOR
0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs3783550
IL1A
0.827 0.200 2 112775308 intron variant G/T snv 0.64 0.70 5
rs3783546
IL1A
0.882 0.160 2 112777253 intron variant G/C snv 0.70 5
rs1609682
IL1A
0.882 0.160 2 112782628 intron variant G/T snv 0.70 3
rs3783521
IL1A
0.807 0.200 2 112786000 upstream gene variant G/A snv 0.26 8