Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs121913281
PIK3CA
0.623 0.520 3 179234296 missense variant C/T snv 37
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 28
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs6471
CYP21A2
0.683 0.360 6 32040110 missense variant G/A;C;T snv 1.2E-05; 5.3E-03 24
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs11554273
GNAS
0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 22
rs1057519932
PIK3CA
0.683 0.320 3 179234298 missense variant T/G snv 22
rs121913409
CTNNB1
0.708 0.400 3 41224646 missense variant C/A;G;T snv 21
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 20
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 19
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 19