Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
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
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs2227983
EGFR
0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 16
rs1213469537
CAV1
0.882 0.080 7 116559145 missense variant C/T snv 4.0E-06 1.4E-05 9
rs387906698
PRSS1
0.827 0.040 7 142751919 missense variant C/A;T snv 4.0E-06; 7.2E-05 8
rs751295137
EGFR
0.851 0.160 7 55152582 missense variant G/A snv 8.0E-06 7.0E-06 6
rs760101437
EGFR
0.851 0.160 7 55154018 missense variant G/A snv 3.2E-05 1.4E-05 6
rs374733251
MET
0.882 0.080 7 116740993 missense variant A/G snv 6.0E-05 7.7E-05 5
rs377444977
EGFR
0.882 0.080 7 55143443 missense variant G/A snv 5.2E-05 2.1E-05 5
rs2069852 0.925 0.080 7 22732641 downstream gene variant G/A;C snv 4
rs121913430
EGFR
1.000 0.080 7 55174740 missense variant G/A snv 3
rs1646724
SLC35B4
0.925 0.080 7 134317123 upstream gene variant T/A;G snv 3
rs1442033697
SERPINE1
7 101135780 frameshift variant A/- del 1
rs1453208391
HGF
7 81707297 missense variant G/A snv 4.0E-06 1
rs531564
LINC00599 ; MIR124-1
0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs2289937
RAD21
0.882 0.080 8 116861572 intron variant G/A;C snv 4
rs4570
UTP23 ; RAD21
0.882 0.080 8 116846150 3 prime UTR variant G/A snv 0.70 4
rs4579555
RAD21
0.882 0.080 8 116867092 intron variant A/G snv 4