Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 19
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 19
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 18
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 17
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 17
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 17
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 16
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 16
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16
rs121912657
TP53
0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 15
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 15
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 14
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs1057519977
TP53
0.763 0.360 17 7675189 missense variant G/C snv 13
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 13