Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587781991
TP53
0.724 0.240 17 7675208 missense variant C/A;T snv 14
rs1057519940
PIK3CA
0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 13
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 13
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 13
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 13
rs28931589
CTNNB1
0.695 0.240 3 41224613 missense variant G/A;C;T snv 13
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 13
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 12
rs1057519896
FBXW7
0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs1057519999
TP53
0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs1057520006
TP53
0.752 0.240 17 7673799 missense variant A/C;G;T snv 12
rs121913272
PIK3CA
0.752 0.400 3 179210192 missense variant T/C;G snv 12
rs121913287
PIK3CA
0.752 0.400 3 179199088 missense variant G/A snv 12
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv 12
rs398124146
CREBBP
0.742 0.360 16 3738617 missense variant G/A;C snv 12
rs587777790
PIK3CA
0.732 0.280 3 179199690 missense variant G/A snv 12
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs866987936
FBXW7
0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519884
CREBBP
0.752 0.240 16 3738616 missense variant C/A;T snv 11
rs1057519886
CTNNB1
0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs1057519933
PIK3CA
0.790 0.240 3 179199156 missense variant A/G snv 11