Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 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
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 28
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 24
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 24
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 23
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 22
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 22
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 21
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21