Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs760101437
EGFR
0.851 0.160 7 55154018 missense variant G/A snv 3.2E-05 1.4E-05 6
rs1050171
EGFR ; EGFR-AS1
0.851 0.120 7 55181370 missense variant G/A;C snv 0.52; 4.0E-06 6
rs1057519860
EGFR
0.851 0.080 7 55160316 missense variant C/A snv 5
rs11979158
EGFR
0.882 0.040 7 55091656 intron variant A/G;T snv 0.20 5
rs1408630981
EGFR
0.827 0.120 7 55205492 missense variant C/G snv 4.0E-06 5
rs377444977
EGFR
0.882 0.080 7 55143443 missense variant G/A snv 5.2E-05 2.1E-05 5
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
rs104886026
EGFR
0.851 0.080 7 55200333 missense variant G/A snv 4
rs11506105
EGFR
0.851 0.160 7 55152484 intron variant A/G snv 0.59 4
rs1171287261
EGFR
0.851 0.080 7 55191839 missense variant G/A snv 4
rs1276184054
EGFR
0.851 0.080 7 55201305 missense variant G/A snv 4.0E-06 4
rs139429793
EGFR
0.925 0.120 7 55155928 missense variant G/A snv 1.6E-05 1.4E-05 4
rs140516819
EGFR
7 55172999 missense variant A/C;G snv 4.0E-05 2.4E-04 4
rs149006234
EGFR
0.851 0.080 7 55146649 synonymous variant G/A;T snv 4.0E-06; 8.0E-06 4
rs2293347
EGFR
0.851 0.080 7 55201223 synonymous variant C/T snv 0.14 9.5E-02 4
rs35918369
EGFR
7 55205613 missense variant C/T snv 3.1E-04 3.3E-04 4
rs397517096
EGFR
0.851 0.120 7 55174776 missense variant TT/CC mnv 4
rs397517097
EGFR
0.851 0.080 7 55174777 missense variant T/C snv 4
rs59060240
EGFR
0.882 0.040 7 55080369 intron variant AA/-;A;AAA;AAAA;AAAAAAAAAAA delins 4
rs723527
EGFR
0.882 0.040 7 55067179 intron variant A/G snv 0.53 4
rs750713244
EGFR
0.925 0.200 7 55157753 missense variant A/G snv 8.0E-06 4
rs776375114
EGFR
0.851 0.080 7 55202577 missense variant G/A;C snv 4.0E-06; 4.0E-06 4
rs866460345
EGFR
0.882 0.120 7 55143362 missense variant C/T snv 4
rs1032006770
EGFR
0.882 0.080 7 55160171 missense variant A/G snv 4.0E-06 7.0E-06 3