Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs1057520009
XPO1
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs111724149
PRDM11
0.925 0.120 11 45204720 missense variant A/G snv 1.8E-03 1.8E-03 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs1178732315
GBA
0.882 0.240 1 155236381 missense variant A/G snv 1.4E-05 3
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913238
KRAS
0.732 0.240 12 25227343 missense variant G/C;T snv 17
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs121913254
NRAS
0.658 0.440 1 114713909 stop gained G/A;C;T snv 31
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913496
LRRC56 ; HRAS
0.724 0.440 11 533873 missense variant C/A;G;T snv 16
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1227230819
GDNF ; GDNF-AS1
0.925 0.120 5 37815877 missense variant T/C snv 4.0E-06 2
rs1239470707
PPARG
0.925 0.120 3 12416785 missense variant C/A snv 2
rs12917
MGMT ; LOC105378560
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs1312391542
ATG5 ; PRDM1
0.925 0.120 6 106104897 missense variant G/A;T snv 2
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1390458638
ABCB6
0.925 0.120 2 219216441 missense variant G/A snv 4.0E-06 2
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27