Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1032006770
EGFR
0.882 0.080 7 55160171 missense variant A/G snv 4.0E-06 7.0E-06 3
rs1032737355
EGFR
0.925 0.080 7 55170434 missense variant T/A snv 2
rs10488140
EGFR
1.000 0.040 7 55070695 intron variant C/T snv 0.26 1
rs104886026
EGFR
0.851 0.080 7 55200333 missense variant G/A snv 4
rs1050171
EGFR ; EGFR-AS1
0.851 0.120 7 55181370 missense variant G/A;C snv 0.52; 4.0E-06 6
rs1051753269
EGFR
0.790 0.120 7 55174029 missense variant G/A snv 7.0E-06 7
rs1057519760
EGFR
7 55160314 missense variant A/G snv 1
rs1057519794
EGFR
0.925 0.080 7 55173927 missense variant G/A snv 2
rs1057519828
EGFR
7 55143387 missense variant G/A snv 1
rs1057519829
EGFR
7 55154050 missense variant A/C;G snv 4.0E-06 1
rs1057519830
EGFR
1.000 0.040 7 55163737 missense variant C/T snv 3
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
rs1057519860
EGFR
0.851 0.080 7 55160316 missense variant C/A snv 5
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs1057519887
EGFR
0.925 0.040 7 55154128 missense variant GC/AA;AT mnv 3
rs1057519888
EGFR
0.925 0.080 7 55143386 missense variant A/G snv 3
rs1057520037
EGFR
1.000 0.080 7 55174782 missense variant G/C snv 1
rs1140476
EGFR
0.925 0.080 7 55200396 missense variant C/T snv 2
rs114972508
EGFR ; LOC105375284
0.925 0.120 7 55020815 intron variant T/C snv 1.4E-02 2
rs11506105
EGFR
0.851 0.160 7 55152484 intron variant A/G snv 0.59 4
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
rs1171287261
EGFR
0.851 0.080 7 55191839 missense variant G/A snv 4
rs1171516758
EGFR
1.000 0.040 7 55142377 synonymous variant G/A;T snv 4.0E-06; 4.0E-06 1