Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 33
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26
rs121913275
PIK3CA
0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 23
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 24
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 24
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs1899663
HOTAIR
0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 24
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 22
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 20
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 20