Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2072454
EGFR
0.763 0.160 7 55146655 synonymous variant C/T snv 0.51 0.51 9
rs730437
EGFR
0.925 0.120 7 55147325 intron variant A/C snv 0.51 2
rs11506105
EGFR
0.851 0.160 7 55152484 intron variant A/G snv 0.59 4
rs1372330611
EGFR
1.000 0.080 7 55152564 missense variant C/G snv 4.0E-06 1
rs751295137
EGFR
0.851 0.160 7 55152582 missense variant G/A snv 8.0E-06 7.0E-06 6
rs759106015
EGFR
7 55152588 missense variant G/A snv 3.2E-05 1.4E-05 1
rs760101437
EGFR
0.851 0.160 7 55154018 missense variant G/A snv 3.2E-05 1.4E-05 6
rs149840192
EGFR
0.807 0.080 7 55154129 missense variant C/A;T snv 5
rs1203030830
EGFR
0.882 0.120 7 55155873 synonymous variant T/C snv 4.0E-06 3
rs775800262
EGFR
1.000 0.080 7 55155894 missense variant G/T snv 4.0E-06 1
rs758748662
EGFR
1.000 0.160 7 55155911 missense variant G/A snv 4.0E-06 1.4E-05 1
rs144460286
EGFR
0.925 0.080 7 55155922 missense variant A/C snv 4.0E-06 2
rs777342222
EGFR
1.000 0.080 7 55155925 missense variant T/C snv 4.0E-06 1
rs139429793
EGFR
0.925 0.120 7 55155928 missense variant G/A snv 1.6E-05 1.4E-05 3
rs771929085
EGFR
1.000 0.160 7 55155941 missense variant G/A snv 1.2E-05 1
rs771398183
EGFR
1.000 0.040 7 55156554 missense variant G/T snv 4.0E-06 1.4E-05 1
rs774905136
EGFR
7 55156555 synonymous variant T/C snv 5.6E-05 1.4E-05 1
rs1405999227
EGFR
0.925 0.160 7 55156637 missense variant A/G snv 4.0E-06 3
rs1389500636
EGFR
0.827 0.080 7 55156796 missense variant G/A snv 6
rs763830096
EGFR
1.000 0.120 7 55157724 synonymous variant A/G snv 4.0E-06 1
rs750713244
EGFR
0.925 0.200 7 55157753 missense variant A/G snv 8.0E-06 4
rs765091640
EGFR
7 55160165 missense variant G/A snv 1.2E-05 1
rs1032006770
EGFR
0.882 0.080 7 55160171 missense variant A/G snv 4.0E-06 7.0E-06 3
rs377567759
EGFR
7 55160191 missense variant C/T snv 4.0E-06 7.0E-06 1
rs746763556
EGFR
7 55160230 missense variant T/A;G snv 1.6E-05; 4.0E-06 2