Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs781490101
TP53
0.851 0.040 17 7673748 missense variant T/C snv 8.0E-06 5
rs12752552
RAVER2
0.882 0.040 1 64763616 intron variant T/C snv 0.13 4
rs1306185959
FGFR1
0.851 0.040 8 38429805 missense variant T/C snv 7.0E-06 4
rs28357681
ND6 ; CYTB
0.851 0.040 MT 14798 missense variant T/C snv 4
rs3851634
POLR3B
0.882 0.040 12 106419124 intron variant T/C snv 0.22 4
rs6062302
RTEL1 ; RTEL1-TNFRSF6B
0.882 0.040 20 63689615 synonymous variant T/C snv 0.74 0.81 4
rs755794544
PDGFA
0.851 0.040 7 512435 missense variant T/C snv 4.0E-06 4
rs9642393
EGFR
0.925 0.040 7 55177954 intron variant T/C snv 0.24 2
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs121913284
PIK3CA
0.776 0.160 3 179203765 missense variant T/A;G snv 11
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 22
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 21
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 19
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 14
rs2243248
IL4
0.763 0.240 5 132672952 upstream gene variant T/A;C;G snv 9
rs10852606
HEATR3
0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs751859698
MSH4
0.925 0.040 1 75898031 missense variant T/A;C snv 1.2E-05 2
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 17
rs1057519995
TP53
0.807 0.240 17 7674200 missense variant T/A snv 9
rs17296479 0.851 0.040 5 81411157 non coding transcript exon variant T/A snv 9.4E-02 5