Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6970262
EGFR
1.000 0.040 7 55192070 intron variant A/G snv 0.66 1
rs729969
EGFR
1.000 0.040 7 55060514 intron variant A/G;T snv 1
rs759165
EGFR
1.000 0.080 7 55049014 intron variant G/A snv 4.3E-02 1
rs845552
EGFR
1.000 0.040 7 55177814 intron variant A/G snv 0.43 1
rs845561
EGFR ; EGFR-AS1
1.000 0.040 7 55185015 intron variant C/T snv 0.76 1
rs9642391
EGFR
1.000 0.080 7 55177671 intron variant G/C snv 0.24 1
rs748491031
EGFR
0.827 0.120 7 55200384 stop gained C/G;T snv 1.2E-05 8
rs121913467
EGFR
1.000 0.080 7 55174730 stop gained G/A snv 1
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
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs2227983
EGFR
0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 11
rs28929495
EGFR
0.807 0.120 7 55174014 missense variant G/A;C;T snv 9
rs397517108
EGFR ; EGFR-AS1
0.790 0.120 7 55181312 missense variant GC/TT mnv 9
rs146795390
EGFR
0.827 0.080 7 55191776 missense variant G/A snv 8.0E-06 7.0E-06 8
rs909797662
EGFR
0.790 0.120 7 55191837 missense variant G/A snv 8
rs1051753269
EGFR
0.790 0.120 7 55174029 missense variant G/A snv 7.0E-06 7
rs11543848
EGFR
0.790 0.240 7 55161562 missense variant G/A;C;T snv 7
rs1169803481
EGFR
0.807 0.160 7 55198851 missense variant A/G snv 4.0E-06 7
rs149840192
EGFR
0.807 0.080 7 55154129 missense variant C/A;T snv 7