Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 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
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 55
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 45
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 44
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1444669684
CDKN2B-AS1 ; CDKN2A
0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 36
rs2853669
TERT
0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 32
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 28
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs11134527
MIR218-2 ; SLIT3
0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 24
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 23
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 20
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 20