Source: BEFREE

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
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs2227983
EGFR
0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs11543848
EGFR
0.790 0.240 7 55161562 missense variant G/A;C;T snv 7
rs750713244
EGFR
0.925 0.200 7 55157753 missense variant A/G snv 8.0E-06 4
rs147740818
EGFR
0.925 0.200 7 55142324 missense variant A/G snv 2
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 17
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 9
rs2072454
EGFR
0.763 0.160 7 55146655 synonymous variant C/T snv 0.51 0.51 9
rs1169803481
EGFR
0.807 0.160 7 55198851 missense variant A/G snv 4.0E-06 7
rs760101437
EGFR
0.851 0.160 7 55154018 missense variant G/A snv 3.2E-05 1.4E-05 6
rs751295137
EGFR
0.851 0.160 7 55152582 missense variant G/A snv 8.0E-06 7.0E-06 6
rs778985185
EGFR
0.851 0.160 7 55163734 missense variant G/A snv 8.0E-06 3.5E-05 5
rs884225
EGFR
0.827 0.160 7 55206391 3 prime UTR variant T/C;G snv 5
rs11506105
EGFR
0.851 0.160 7 55152484 intron variant A/G snv 0.59 4
rs13222385
EGFR-AS1 ; EGFR
1.000 0.160 7 55183900 intron variant A/G snv 0.28 3
rs773454677
EGFR
0.925 0.160 7 55205466 missense variant G/A snv 1.2E-05 3
rs1405999227
EGFR
0.925 0.160 7 55156637 missense variant A/G snv 4.0E-06 3
rs121913418
EGFR
0.882 0.160 7 55174818 missense variant G/A;T snv 2
rs771366736
EGFR
1.000 0.160 7 55143380 missense variant A/G snv 8.0E-06 1.4E-05 1
rs758748662
EGFR
1.000 0.160 7 55155911 missense variant G/A snv 4.0E-06 1.4E-05 1
rs771929085
EGFR
1.000 0.160 7 55155941 missense variant G/A snv 1.2E-05 1