Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs727503094
LRRC56 ; HRAS
0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs5742909
CTLA4
0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs121913281
PIK3CA
0.623 0.520 3 179234296 missense variant C/T snv 37
rs4646903
CYP1A1
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs2853669
TERT
0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs689466
PACERR ; PTGS2
0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs1982073
TGFB1
0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs61764370
KRAS
0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs121909219
PTEN
0.689 0.400 10 87957915 stop gained C/A;T snv 25
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs11134527
MIR218-2 ; SLIT3
0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23