Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 26
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 17
rs121913492
GNAQ
0.790 0.160 9 77794572 missense variant T/A;C;G snv 11
rs1057519742
GNA11
0.827 0.160 19 3118944 missense variant A/C;T snv 7
rs387906631
GATA2
0.882 0.080 3 128481901 missense variant G/A snv 6
rs118203900
LAMC2
1.000 0.080 1 183228564 stop gained C/A snv 2