Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
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
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 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
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 23
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs1899663
HOTAIR
0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 22
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 20