Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs26532
ATG12
1.000 0.120 5 115837981 non coding transcript exon variant C/A snv 0.83 1
rs17368584
ST6GALNAC5
1.000 0.120 1 76930481 intron variant T/A;C snv 1
rs4760259
GLI1
0.925 0.160 12 57467043 intron variant T/A;C snv 2
rs760112920
KIT
0.925 0.120 4 54731930 missense variant G/T snv 4.0E-06 3.5E-05 2
rs26865
MLST8
0.925 0.160 16 2203772 upstream gene variant A/G snv 0.41 2
rs12913975
SMAD6
0.925 0.160 15 66764823 intron variant G/A snv 0.17 2
rs3160
BRICD5 ; MLST8
0.925 0.160 16 2209190 3 prime UTR variant T/C snv 0.36 3
rs121913418
EGFR
0.882 0.160 7 55174818 missense variant G/A;T snv 3
rs10036653
ATG10
0.851 0.160 5 81970563 upstream gene variant A/T snv 0.17 4
rs763375936
ATG3
0.827 0.160 3 112532749 missense variant C/T snv 8.3E-06 7.0E-06 5
rs772776695
ATG3
0.827 0.160 3 112548576 missense variant T/A snv 4.0E-06 5
rs751688663
ATG7
0.807 0.280 3 11340656 missense variant G/A snv 4.0E-06 7
rs763538721
HIF1A-AS3 ; HIF1A
0.807 0.160 14 61740897 missense variant T/A snv 4.0E-06 8
rs2494732
AKT1
0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs2699887
PIK3CA ; LOC101928739
0.763 0.280 3 179148620 intron variant C/T snv 0.18 11
rs4803455
TGFB1
0.752 0.280 19 41345604 intron variant C/A snv 0.51 11
rs3809865
THCAT158 ; ITGB3
0.790 0.240 17 47311220 3 prime UTR variant T/A;G snv 11
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
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
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78