Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 21
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 21
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
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 14
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519999
TP53
0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs28934573
TP53
0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 28
rs121912657
TP53
0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 24
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 25
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 22
rs28934574
TP53
0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 31
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 23
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1057519974
ELOC
1.000 0.120 8 73946734 missense variant A/T snv 1
rs1057519973
ELOC
1.000 0.120 8 73946733 missense variant T/A;G snv 1