Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs775514340
CILK1
0.882 0.080 6 53041202 missense variant T/A;C snv 4.0E-06 5
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1238968510
MMP2
0.882 0.080 16 55479556 missense variant A/G;T snv 4.1E-06 2.1E-05 4
rs8021944
ESR2 ; SYNE2
14 64212580 intron variant T/G snv 5.6E-02 1
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 5
rs10146204 1.000 0.120 14 64352051 non coding transcript exon variant G/A snv 0.45 2
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 23
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs588765
CHRNA5
0.827 0.200 15 78573083 intron variant T/A;C snv 6
rs3743073
CHRNA3
0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs199976573
ABCG2
0.925 0.120 4 88132618 missense variant C/T snv 6.4E-05 5.6E-05 4