Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs150036236
EGFR
0.925 0.080 7 55191741 missense variant G/A snv 4.8E-05 3.5E-05 2
rs397517097
EGFR
0.851 0.080 7 55174777 missense variant T/C snv 2
rs730881972
STK11
1.000 0.080 19 1220395 missense variant G/C;T snv 2
rs1057519789
DDR2
1.000 0.080 1 162775707 missense variant A/G;T snv 4.0E-06 1
rs1057519790
DDR2
1.000 0.080 1 162778617 missense variant G/T snv 1
rs1057519791
FGFR2
1.000 0.080 10 121518810 missense variant G/C snv 1
rs121913376
BRAF
0.925 0.080 7 140781597 missense variant C/A;T snv 1
rs144594252
DDR2
0.882 0.080 1 162754625 missense variant C/G snv 6.8E-05 5.6E-05 1
rs34192549
EPHA2
1.000 0.080 1 16137994 missense variant C/G;T snv 2.5E-02 1
rs376303676
DDR2
1.000 0.080 1 162759881 missense variant G/A;T snv 8.0E-06 1
rs578015216
DDR2
1.000 0.080 1 162759840 missense variant T/C;G snv 2.8E-05 1
rs764449808
STK11
1.000 0.080 19 1218494 missense variant A/G snv 1.2E-05 3.5E-05 1
rs121913386
CDKN2A
0.807 0.120 9 21971018 missense variant G/A;T snv 6
rs121913428
EGFR
0.827 0.120 7 55174015 missense variant G/A;C snv 4
rs763733111
PPP6C
0.925 0.120 9 125149801 missense variant G/A snv 4.0E-06 2
rs1057519920
NFE2L2
0.790 0.160 2 177234232 missense variant C/A;G;T snv 7
rs749415085
PIK3CA
0.807 0.160 3 179198937 missense variant C/A;G;T snv 7
rs1057519931
PIK3CA
0.827 0.160 3 179199141 missense variant G/C snv 6
rs772110575
PIK3CA
0.807 0.160 3 179198938 missense variant G/A;T snv 4.0E-06 6
rs104894104
CDKN2A
0.790 0.160 9 21971019 missense variant G/A;T snv 4
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 3
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 3
rs121918499
FGFR2
0.925 0.160 10 121520048 missense variant C/A;G snv 2
rs1057519926
PIK3CA
0.776 0.200 3 179210293 missense variant A/T snv 10
rs1057519928
PIK3CA
0.807 0.200 3 179221147 missense variant A/C snv 8