Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894340
CDK4
0.827 0.200 12 57751647 missense variant C/A;T snv 1
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 3
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 2
rs104894097
CDKN2A
0.807 0.240 9 21974757 missense variant C/A;G;T snv 1.7E-05; 1.3E-05 1
rs121913113
FGFR3
0.882 0.240 4 1806076 missense variant G/A snv 1
rs121913375
BRAF
0.851 0.240 7 140753339 missense variant G/A;C snv 1
rs121913407
CTNNB1
0.763 0.240 3 41224645 missense variant T/C;G snv 1
rs121913514
KIT
0.763 0.240 4 54733174 missense variant T/A;G snv 1
rs28931589
CTNNB1
0.695 0.240 3 41224613 missense variant G/A;C;T snv 1
rs45580035
BRCA2
0.790 0.240 13 32380043 missense variant C/T snv 1.2E-05 1
rs121913341
BRAF
0.851 0.280 7 140753350 missense variant A/C;T snv 2
rs121913361
BRAF
0.807 0.280 7 140753349 missense variant C/A;G;T snv 1
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 1
rs36053993
MUTYH
0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 1
rs387906659
AKT2
0.742 0.280 19 40257052 stop gained C/A;T snv 1
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 2
rs121913506
KIT
0.677 0.320 4 54733154 missense variant G/A;C;T snv 2
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 2
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 1
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 1
rs11547328
CDK4
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 1
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 1
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 2
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 1