Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17172432
EGFR
0.882 0.080 7 55073624 intron variant T/C snv 0.31 3
rs781609053
EGFR
0.925 0.120 7 55200379 missense variant T/C snv 1.2E-05 3
rs867182279
EGFR
0.882 0.080 7 55205510 missense variant T/C snv 3
rs770443325
EGFR
0.882 0.080 7 55172994 missense variant C/G;T snv 2.8E-05 3
rs148934350
EGFR
0.882 0.080 7 55191792 missense variant C/A;T snv 8.0E-06; 3.6E-04 3
rs727504256
EGFR
0.882 0.080 7 55173984 missense variant G/A snv 8.0E-06 3
rs763317
EGFR
0.882 0.080 7 55027504 intron variant A/G snv 0.59 3
rs757699239
EGFR
0.882 0.080 7 55201269 missense variant G/A;C snv 8.0E-06; 4.0E-06 3
rs1420841957
EGFR
0.882 0.080 7 55201275 missense variant G/C snv 4.0E-06 7.0E-06 3
rs1405999227
EGFR
0.925 0.160 7 55156637 missense variant A/G snv 4.0E-06 3
rs780439043
EGFR
0.925 0.080 7 55205301 missense variant A/G snv 8.0E-06 1.4E-05 3
rs13222385
EGFR-AS1 ; EGFR
1.000 0.160 7 55183900 intron variant A/G snv 0.28 3
rs6965469
EGFR ; LOC105375284
0.882 0.080 7 55017274 upstream gene variant C/A;T snv 3
rs730437
EGFR
0.925 0.120 7 55147325 intron variant A/C snv 0.51 2
rs1468727
EGFR
0.925 0.120 7 55162412 intron variant C/T snv 0.21 2
rs1334180707
EGFR
0.925 0.080 7 55161510 missense variant C/G snv 4.0E-06 2
rs1140476
EGFR
0.925 0.080 7 55200396 missense variant C/T snv 2
rs746763556
EGFR
7 55160230 missense variant T/A;G snv 1.6E-05; 4.0E-06 2
rs987532315
EGFR
7 55201782 splice region variant G/A snv 4.0E-06 2
rs147740818
EGFR
0.925 0.200 7 55142324 missense variant A/G snv 2
rs1032737355
EGFR
0.925 0.080 7 55170434 missense variant T/A snv 2
rs1219568637
EGFR
7 55143404 missense variant G/A snv 7.0E-06 2
rs756703787
EGFR
1.000 0.080 7 55191845 missense variant G/A snv 4.0E-06 2
rs1282801317
EGFR
0.925 0.080 7 55143316 missense variant G/C snv 4.0E-06 2
rs9642393
EGFR
0.925 0.040 7 55177954 intron variant T/C snv 0.24 2