Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs1057519946
PPP2R1A
0.732 0.280 19 52212729 missense variant C/G;T snv 18
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 17
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs587781991
TP53
0.724 0.240 17 7675208 missense variant C/A;T snv 17
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs1057519942
PIK3CA
0.724 0.320 3 179203760 missense variant G/A snv 16
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 16
rs121913496
LRRC56 ; HRAS
0.724 0.440 11 533873 missense variant C/A;G;T snv 16
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 16
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 16
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 15
rs587780071
TP53
0.732 0.240 17 7674951 missense variant G/A snv 15
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 15
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 15
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 14
rs1057520005
TP53
0.742 0.360 17 7673800 missense variant C/A;G snv 14
rs1057520006
TP53
0.752 0.240 17 7673799 missense variant A/C;G;T snv 14
rs377767347
SMAD4
0.742 0.520 18 51065549 missense variant G/A;C;T snv 14
rs587777790
PIK3CA
0.732 0.280 3 179199690 missense variant G/A snv 14