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
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
rs2072454
EGFR
0.763 0.160 7 55146655 synonymous variant C/T snv 0.51 0.51 9
rs149840192
EGFR
0.807 0.080 7 55154129 missense variant C/A;T snv 7
rs1389500636
EGFR
0.827 0.080 7 55156796 missense variant G/A snv 6
rs1276184054
EGFR
0.851 0.080 7 55201305 missense variant G/A snv 4.0E-06 4
rs776375114
EGFR
0.851 0.080 7 55202577 missense variant G/A;C snv 4.0E-06; 4.0E-06 4
rs1057519830
EGFR
1.000 0.040 7 55163737 missense variant C/T snv 3
rs1057519887
EGFR
0.925 0.040 7 55154128 missense variant GC/AA;AT mnv 3
rs769696078
EGFR
0.925 0.040 7 55154128 missense variant G/A snv 3
rs754426793
EGFR-AS1 ; EGFR
0.925 0.080 7 55181395 missense variant G/A snv 1.2E-05 1.4E-05 2
rs121913433
EGFR
1.000 0.040 7 55174771 missense variant A/G snv 1
rs1256743514
EGFR
1.000 0.040 7 55191728 missense variant T/C snv 7.0E-06 1
rs6970262
EGFR
1.000 0.040 7 55192070 intron variant A/G snv 0.66 1
rs845561
EGFR ; EGFR-AS1
1.000 0.040 7 55185015 intron variant C/T snv 0.76 1