Disease: Neoplasms
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9904341
BIRC5
0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs9600079 0.925 0.080 13 73154002 intergenic variant G/T snv 0.46 5
rs937283
MDM2
0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs9350
EXO1
0.742 0.240 1 241885372 missense variant C/T snv 0.21 0.19 16
rs931127
SIPA1 ; PCNX3
0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs9282861
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 31
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs917570055
GZMM
0.882 0.360 19 547342 start lost A/G snv 7
rs917411291
GZMM
0.851 0.360 19 544072 start lost A/C;G snv 9
rs9138
SPP1
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv 12
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs876660427
APC
5 112838608 missense variant C/T snv 4
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs873601
BIVM-ERCC5 ; ERCC5
0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 16
rs868047715
KDR
4 55089696 missense variant G/A snv 3
rs867114783
TP53
17 7675109 missense variant T/C snv 6
rs864622017
E2F1
20 33679830 missense variant C/T snv 3
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs80357610
BRCA1
0.851 0.160 17 43094550 frameshift variant GT/- delins 7
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 29
rs796065354
ESR1
0.882 0.080 6 151944320 missense variant A/G snv 9