Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 1
rs11554273
GNAS
0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 1
rs121913385
CDKN2A
0.763 0.240 9 21971112 missense variant G/A;C snv 1
rs121913407
CTNNB1
0.763 0.240 3 41224645 missense variant T/C;G snv 1
rs121913469
ERBB2
0.763 0.240 17 39723966 missense variant TT/CC mnv 1
rs147001633
DNMT3A
0.776 0.240 2 25234373 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.2E-04 1
rs28931589
CTNNB1
0.695 0.240 3 41224613 missense variant G/A;C;T snv 1
rs377577594
DNMT3A
0.827 0.240 2 25234374 missense variant G/A;C;T snv 1.2E-04; 8.0E-06 1
rs786203071
TP53
0.776 0.240 17 7675181 missense variant T/A;G snv 1
rs879254046
ATM
0.925 0.240 11 108267246 stop gained G/A;C;T snv 1
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 1
rs121912580
SMAD4
0.807 0.280 18 51067036 missense variant G/A;C;T snv 1
rs121913361
BRAF
0.807 0.280 7 140753349 missense variant C/A;G;T snv 1
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 1
rs80338963
SMAD4
0.776 0.280 18 51065548 missense variant C/A;G;T snv 1
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 1
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
rs1057519929
PIK3CA
0.776 0.320 3 179199066 missense variant G/A snv 1
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 1
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 1
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 1
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 1
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 4
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs104894231
LRRC56 ; HRAS
0.776 0.360 11 533467 missense variant C/G;T snv 1