Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs4646903
CYP1A1
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs3742330
DICER1
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 12
rs28366003
MT2A
0.763 0.240 16 56608579 upstream gene variant A/C;G snv 4.6E-02 10
rs115160714
TOPBP1
0.807 0.200 3 133601021 3 prime UTR variant G/A snv 5.8E-03 9
rs6877842
DROSHA ; C5orf22
0.807 0.320 5 31532531 intron variant G/C snv 0.16 7
rs13078
DICER1
0.827 0.280 14 95090410 3 prime UTR variant A/T snv 0.85 5
rs5744455
CD14 ; TMCO6
0.882 0.160 5 140633722 upstream gene variant G/A;T snv 5
rs4789223
SMIM6 ; RECQL5
0.851 0.120 17 75645819 intron variant G/A snv 0.46 4
rs1816158
MIR100HG
0.925 0.200 11 122155752 intron variant C/A;T snv 3
rs3213282
XRCC1
0.882 0.160 19 43568728 intron variant G/C snv 0.57 3
rs3810378
XRCC1 ; PINLYP
1.000 0.120 19 43577449 intron variant G/C snv 0.29 3
rs4725443
KMT2C
0.925 0.120 7 152170176 intron variant T/C snv 9.3E-02 2
rs50871
ERCC2
0.925 0.120 19 45359257 intron variant C/A snv 0.64 2
rs56161233
SH3BP4
0.925 0.120 2 235055489 3 prime UTR variant C/T snv 0.11 2
rs6943984
KMT2C
0.925 0.120 7 152201919 intron variant G/A snv 0.11 2
rs1799778
XRCC1
1.000 0.120 19 43554989 intron variant G/T snv 0.31 1
rs865789884
TNFRSF10D
0.925 0.120 8 23145778 missense variant G/A;C snv 4.0E-06 2
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs748148861
CCR6
0.925 0.120 6 167136856 missense variant G/C snv 8.0E-06 2