Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs9370729 6 14138061 downstream gene variant C/T snv 0.44 1
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs863225307
APC
5 112819077 stop gained C/T snv 1
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs8305
POLI
0.882 0.120 18 54294435 missense variant G/A snv 0.72 0.78 4
rs8038415
IGF1R
15 98956205 intron variant T/C snv 0.58 1
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
rs782212015
CEACAM5
19 41721077 missense variant G/A snv 8.0E-06 2.1E-05 1
rs779577244
LOC107984219 ; KIF5B
10 32017334 missense variant C/A snv 4.0E-06 1
rs778826879
MAPK3
16 30121948 missense variant C/G;T snv 1.2E-05; 8.0E-06 3
rs767808984
NKX2-1-AS1 ; SFTA3 ; NKX2-1
0.851 0.160 14 36520098 missense variant C/G;T snv 1.3E-05 9
rs766779326
ESR1
1.000 0.040 6 151944344 missense variant C/T snv 4.0E-06 7.0E-06 2
rs765660823
DDR2
0.882 0.200 1 162778720 missense variant A/C snv 1.9E-04 4
rs764664272
MMP2
1.000 0.120 16 55484060 missense variant A/G snv 1.2E-05 7.0E-06 2
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs759435862
KIDINS220
0.925 0.080 2 8776852 missense variant C/A;T snv 2.0E-05 5
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs755683317
TPTE
21 10567746 missense variant G/A;C snv 2.4E-05 3
rs754332870
TP53
0.790 0.240 17 7676240 missense variant C/G snv 4.0E-06 9
rs753152604
CDK4
0.827 0.040 12 57751680 missense variant C/A snv 7
rs752021744
PIK3CB
0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs751144688
CD44
1.000 0.080 11 35206195 missense variant C/T snv 4.0E-06 4
rs750749 6 14141866 downstream gene variant T/C snv 0.27 1