Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs869025608
MAP2K1
0.763 0.400 15 66435117 missense variant G/C;T snv 9
rs868438023
KNSTRN
0.882 0.080 15 40382906 missense variant C/T snv 2
rs866987936
FBXW7
0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 19
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs80338796
RAF1
0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 35
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 19
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs775623976
SF3B1
0.851 0.240 2 197402760 missense variant G/A;C snv 4.0E-06 4
rs770248150
KRAS
0.807 0.240 12 25225713 missense variant T/A;G snv 4.0E-06 6
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs763733111
PPP6C
0.925 0.120 9 125149801 missense variant G/A snv 4.0E-06 2
rs759610249
FBXW7
0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs756091827
MYC ; CASC11
0.851 0.200 8 127738435 missense variant C/G;T snv 6
rs754688962
SF3B1
0.851 0.200 2 197402637 missense variant T/C;G snv 5
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs750664148
CASC11 ; MYC
0.851 0.200 8 127738434 missense variant A/C;G snv 5
rs747241612
FBXW7
0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23