Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 23
rs1057519932
PIK3CA
0.683 0.320 3 179234298 missense variant T/G snv 22
rs879255280
SMO
0.701 0.200 7 129206557 missense variant C/T snv 22
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 19
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 17
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 17
rs28931588
CTNNB1
0.701 0.200 3 41224606 missense variant G/A;C;T snv 17
rs28931589
CTNNB1
0.695 0.240 3 41224613 missense variant G/A;C;T snv 17
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 17
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 16
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs41293497
BRCA2
0.724 0.440 13 32340037 stop gained C/A;G;T snv 4.0E-06; 2.0E-05 14
rs80358721
BRCA2
0.724 0.320 13 32339320 stop gained C/A;G;R snv 4.2E-06 14
rs80358920
BRCA2
0.732 0.400 13 32346841 stop gained C/G;T snv 14
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs867384286
FBXW7
0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs3734254
PPARD
0.752 0.240 6 35427233 3 prime UTR variant C/T snv 0.69 14
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 13
rs121913399
CTNNB1
0.724 0.200 3 41224612 missense variant G/A;C snv 13
rs1057519940
PIK3CA
0.752 0.200 3 179218308 missense variant G/T snv 13
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs80358814
BRCA2
0.742 0.440 13 32340212 stop gained G/T snv 8.0E-06 12
rs80358972
BRCA2
0.742 0.480 13 32356472 stop gained C/A;T snv 8.0E-06; 3.2E-05 12
rs80359200
BRCA2
0.752 0.320 13 32394726 stop gained C/A;G snv 8.0E-06 12