Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 3
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs869025608
MAP2K1
0.763 0.400 15 66435117 missense variant G/C;T snv 9
rs867384286
FBXW7
0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs867262025
PIK3CA
0.790 0.360 3 179221146 missense variant G/A snv 9
rs866987936
FBXW7
0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
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
rs80338963
SMAD4
0.776 0.280 18 51065548 missense variant C/A;G;T snv 11
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs786203071
TP53
0.776 0.240 17 7675181 missense variant T/A;G snv 8
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs786201419
TP53
0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 19