Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
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
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 19
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 19
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs121913485
FGFR3
0.716 0.400 4 1804372 missense variant A/G snv 18
rs121913478
FGFR2
0.708 0.640 10 121515280 missense variant T/C snv 17
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs2151280
CDKN2B-AS1
0.701 0.360 9 22034720 non coding transcript exon variant G/A snv 0.46 16
rs2242652
TERT
0.724 0.400 5 1279913 intron variant G/A snv 0.18 16
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 16
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 16
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 16
rs4135385
CTNNB1
0.742 0.320 3 41237949 non coding transcript exon variant A/G snv 0.19 14
rs603965
CCND1
0.732 0.440 11 69648142 splice region variant G/A snv 14