Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 24
rs2249825
HMGB1
0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs1412125
HMGB1
0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1360485
HMGB1
0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 16
rs4784227
CASC16
0.807 0.160 16 52565276 intron variant C/T snv 0.20 8
rs999737
RAD51B
0.776 0.200 14 68567965 intron variant C/T snv 0.16 8
rs4849887 0.807 0.080 2 120487546 intergenic variant T/A;C snv 7
rs397507758
BRCA2
0.807 0.200 13 32339456 stop gained C/T snv 6
rs4415084 0.827 0.080 5 44662413 upstream gene variant C/T snv 0.49 6
rs9485372
TAB2
0.807 0.120 6 149287738 intron variant G/A snv 0.20 6
rs1054135
FABP4 ; LOC101927118
0.851 0.240 8 81478525 3 prime UTR variant C/T snv 0.17 5
rs10771399 0.827 0.080 12 28002147 intergenic variant A/G snv 8.9E-02 5
rs587779287
FBXO11 ; MSH6
0.827 0.200 2 47806280 frameshift variant GTACATTATTTTC/- delins 5
rs80357367
BRCA1
0.851 0.200 17 43057090 stop gained G/A snv 5
rs1064793184
FBXO11 ; MSH6
0.851 0.080 2 47791055 missense variant A/G snv 4