Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 7
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 5
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 5
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 4
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 4
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 4
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 4
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 3
rs121913413
CTNNB1
0.763 0.240 3 41224634 missense variant C/A;T snv 3
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
rs66904256
ABCB4
0.882 0.080 7 87439777 missense variant T/A snv 2
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 2
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 2
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 2
rs28931588
CTNNB1
0.701 0.200 3 41224606 missense variant G/A;C;T snv 2
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 2
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 2
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 2
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 2
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs387906659
AKT2
0.742 0.280 19 40257052 stop gained C/A;T snv 1
rs863223904
ALAS2
0.827 0.200 X 55014829 missense variant C/T snv 6.1E-06 1
rs116350678
AXIN1
1.000 0.080 16 298233 missense variant C/T snv 4.8E-03 2.3E-02 1