Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35324266 1.000 0.040 6 32625467 upstream gene variant C/T snv 0.16 1
rs62209647 1.000 0.040 20 33917852 upstream gene variant G/C snv 4.4E-02 1
rs6791479 1.000 0.040 3 189487243 intergenic variant T/A snv 0.48 1
rs9557210 1.000 0.040 13 99395250 intergenic variant G/A snv 0.16 1
rs117984432
ANKRD11
1.000 0.040 16 89388583 intron variant T/C snv 2.0E-02 1
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 1
rs1460816
BRCA2
1.000 0.040 13 32354271 intron variant G/A snv 0.54 1
rs987525
CCDC26
0.807 0.160 8 128933908 intron variant C/A snv 0.31 1
rs2230641
CCNH
0.807 0.240 5 87399457 missense variant A/G;T snv 0.18 0.17 1
rs116150891
CDKN2A
1.000 0.040 9 21970929 missense variant G/A;C snv 5.6E-04 2.6E-03 1
rs6413464
CDKN2A
1.000 0.040 9 21970980 missense variant C/A;G snv 1.3E-03; 4.1E-06 1
rs144594252
DDR2
0.882 0.080 1 162754625 missense variant C/G snv 6.8E-05 5.6E-05 1
rs267598140
DDR2
0.925 0.080 1 162778600 missense variant T/A;G snv 1
rs8063761
DEF8
1.000 0.040 16 89961218 intron variant A/T snv 0.33 1
rs9383064
DTNBP1 ; LOC105374947
1.000 0.040 6 15535090 intron variant G/C snv 0.24 1
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 1
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 1
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 1
rs121913230
EGFR ; EGFR-AS1
1.000 0.040 7 55181437 missense variant G/A snv 1
rs121913431
EGFR ; EGFR-AS1
1.000 0.040 7 55181438 missense variant G/A snv 1
rs397517108
EGFR ; EGFR-AS1
0.790 0.120 7 55181312 missense variant GC/TT mnv 1
rs7242481
ELP2 ; SLC39A6
0.925 0.080 18 36129254 5 prime UTR variant G/A snv 0.35 1
rs6743068
FLACC1
1.000 0.040 2 201289197 intron variant A/G snv 0.72 1
rs62246017
FOXP1
1.000 0.040 3 71433933 intron variant G/A;C snv 1
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1