Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs989902
PTPN13
0.742 0.240 4 86785353 missense variant T/G snv 0.42 0.53 12
rs9868873
SEMA5B
1.000 0.080 3 123012063 intron variant G/A snv 0.28 2
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv 7
rs9566910
DGKH
13 42076866 intron variant G/A snv 0.36 1
rs9547991
TRPC4
13 37643278 intron variant T/C snv 0.24 1
rs9288520 2 216616548 intergenic variant G/A snv 0.14 1
rs9288318
FLACC1
2 201331340 intron variant C/A snv 0.63 1
rs917870680
MDM2
0.925 0.080 12 68839304 missense variant A/G snv 3
rs907091
IKZF3
0.851 0.280 17 39765489 3 prime UTR variant C/T snv 0.47 6
rs902907 9 79199649 upstream gene variant G/A snv 0.56 1
rs896570 10 47145727 intergenic variant C/T snv 0.50 1
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs886063150
CA2
0.925 0.080 8 85477151 missense variant C/A;T snv 8.0E-06 3
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 28
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs873601
BIVM-ERCC5 ; ERCC5
0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs861530
LOC112268131 ; XRCC3 ; KLC1
0.732 0.320 14 103707786 3 prime UTR variant T/C snv 0.65 13
rs8103163
ZNF208
0.882 0.120 19 21991950 intron variant A/C snv 0.59 4
rs8057779
WWOX
16 78349243 intron variant C/G snv 0.52 1
rs8030672 1.000 0.080 15 68766745 intergenic variant T/A snv 5.4E-02 2
rs7922612
PLCE1
0.752 0.080 10 94051682 intron variant C/T snv 0.39 14
rs7851133
MTAP
9 21846328 intron variant C/T snv 0.24 1
rs7813
GEMIN4
0.689 0.360 17 744946 missense variant G/A;C snv 0.63 22
rs776933870
PLCE1
0.925 0.080 10 94306632 missense variant A/G snv 8.0E-06 3
rs7763881
HULC ; LOC100506207
0.776 0.160 6 8653014 non coding transcript exon variant A/C snv 0.44 11