Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1341667
STOX1
0.925 0.040 10 68882104 missense variant T/C snv 0.62 0.57 4
rs587782359
CDH1
1.000 0.080 16 68812244 missense variant C/G;T snv 2.8E-05 3
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs937283
MDM2
0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs1373481065
GADD45A
0.827 0.040 1 67687668 missense variant A/G snv 4.0E-06 6
rs1194338 0.925 0.080 11 65493967 upstream gene variant C/A;T snv 3
rs763538721
HIF1A-AS3 ; HIF1A
0.807 0.160 14 61740897 missense variant T/A snv 4.0E-06 8
rs2333227
MPO
0.752 0.320 17 58281401 upstream gene variant C/T snv 0.24 15
rs777009146
CTNND1 ; TMX2-CTNND1
11 57805955 missense variant G/A snv 2.0E-05 2.8E-05 1
rs1022088103
MMP2
16 55485759 missense variant G/A snv 1
rs1231584616
MMP2
16 55485367 missense variant G/A snv 4.0E-06 1
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121913430
EGFR
1.000 0.080 7 55174740 missense variant G/A snv 3
rs2227983
EGFR
0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs760101437
EGFR
0.851 0.160 7 55154018 missense variant G/A snv 3.2E-05 1.4E-05 6
rs751295137
EGFR
0.851 0.160 7 55152582 missense variant G/A snv 8.0E-06 7.0E-06 6
rs377444977
EGFR
0.882 0.080 7 55143443 missense variant G/A snv 5.2E-05 2.1E-05 5
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs35697691
LOC112268150 ; MAPK6
15 52061301 missense variant C/G snv 5.8E-02 5.9E-02 3