Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 17
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 19
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 19
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 16
rs28931588
CTNNB1
0.701 0.200 3 41224606 missense variant G/A;C;T snv 14
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 13
rs121913409
CTNNB1
0.708 0.400 3 41224646 missense variant C/A;G;T snv 9
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
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
rs121913485
FGFR3
0.716 0.400 4 1804372 missense variant A/G snv 8
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 16