Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 17
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
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
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
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T 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
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs1057519942
PIK3CA
0.724 0.320 3 179203760 missense variant G/A snv 15
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 15
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs121912657
TP53
0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 15
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 15
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs121909218
PTEN
0.672 0.360 10 87933145 missense variant G/A snv 14
rs121913283
PIK3CA
0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 14
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 14
rs587781991
TP53
0.724 0.240 17 7675208 missense variant C/A;T snv 14