Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519982
TP53
1.000 0.080 17 7674239 missense variant A/C;G;T snv 1
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 2
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 2
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 13
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 1
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 23
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 1
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 7
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 9
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 4
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 16
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 3
rs587780071
TP53
0.732 0.240 17 7674951 missense variant G/A snv 4
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 1
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 2
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 1
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 9
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 1
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 4
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 1
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 36
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 6
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 4
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 5
rs121912654
TP53
0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 19