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
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs20417
PACERR ; PTGS2
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs3834129
CASP8
0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs763110
FASLG
0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs61764370
KRAS
0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs2695121
NR1H2
0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 16
rs3808607
CYP7A1
0.716 0.400 8 58500365 upstream gene variant G/T snv 0.55 16
rs7922612
PLCE1
0.752 0.080 10 94051682 intron variant C/T snv 0.39 14
rs11954856
APC
0.732 0.200 5 112751630 intron variant T/G snv 0.54 12
rs2486758
CYP17A1
0.742 0.160 10 102837723 upstream gene variant T/C snv 0.18 11
rs3824260
CYP7A1
0.742 0.160 8 58500631 upstream gene variant A/G;T snv 11
rs4791171
AXIN2
0.763 0.080 17 65545379 intron variant T/C snv 0.55 11
rs6557634
TNFRSF10A
0.763 0.080 8 23202743 missense variant T/C snv 11