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
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 4
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 3
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
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 2
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 2
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 2
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 2
rs1291513037
APC
1.000 0.040 5 112839481 missense variant C/T snv 4.0E-06 1
rs878853445
APC
1.000 0.040 5 112840008 missense variant G/A snv 8.0E-06 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs41293511
BRCA2
0.763 0.320 13 32363369 missense variant G/A;C snv 7.0E-06 1
rs80359014
BRCA2
0.763 0.320 13 32362596 missense variant A/G;T snv 1
rs121913399
CTNNB1
0.724 0.200 3 41224612 missense variant G/A;C snv 1
rs28931589
CTNNB1
0.695 0.240 3 41224613 missense variant G/A;C;T snv 1
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 1
rs779707422
FGFR1
0.763 0.280 8 38417331 missense variant G/A;T snv 4.0E-06 1
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 1
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 1
rs61754966
NBN
0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 1
rs1057519929
PIK3CA
0.776 0.320 3 179199066 missense variant G/A snv 1
rs121913281
PIK3CA
0.623 0.520 3 179234296 missense variant C/T snv 1
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 1