Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs750597831
ATM
1.000 0.120 11 108229230 missense variant C/T snv 8.0E-06 7.0E-06 2
rs611646
ATM
0.882 0.120 11 108306370 intron variant T/A;C snv 3
rs587782274
ATM ; C11orf65
1.000 0.120 11 108312465 missense variant A/C snv 1
rs876658517
ATM ; C11orf65
1.000 0.120 11 108327735 missense variant A/G;T snv 1
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
rs1055259
GSTM3 ; GSTM5
1.000 0.120 1 109734239 3 prime UTR variant T/C snv 0.12 1
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
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
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
rs1048798213
APC
1.000 0.120 5 112837872 missense variant C/G snv 1
rs1442780982
APC
1.000 0.120 5 112837977 missense variant C/A;G;T snv 4.0E-06 1
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs2761016
ALAD
0.925 0.120 9 113391072 intron variant T/C snv 0.59 2
rs1800435
ALAD
0.827 0.200 9 113391611 missense variant C/G snv 8.3E-02 6.1E-02 7
rs2606736
ATG7
1.000 0.120 3 11358775 intron variant C/A;T snv 4