Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 19
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 16
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 15
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 13
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 12
rs1057519886
CTNNB1
0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 6
rs1057519728
MAP2K1
0.851 0.120 15 66435103 missense variant T/A;C;G snv 5
rs1057519906
IDH2
0.882 0.120 15 90088607 missense variant T/A;C snv 5
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 1
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 10
rs1057519995
TP53
0.807 0.240 17 7674200 missense variant T/A snv 8
rs1057519890
ERBB2
0.807 0.200 17 39723966 missense variant T/A snv 7
rs1057519940
PIK3CA
0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057519741
SMAD4
18 51078417 missense variant G/T snv 1
rs121913326
APC
5 112839729 stop gained G/T snv 1
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 17
rs1057519943
POLE
0.790 0.160 12 132676598 missense variant G/C;T snv 5
rs121913238
KRAS
0.732 0.240 12 25227343 missense variant G/C;T snv 3
rs121913236
KRAS
0.882 0.160 12 25245321 missense variant G/C;T snv 1