Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs397514644
AKT1
0.925 0.040 14 104780190 missense variant G/A snv 7.0E-06 1
rs387906659
AKT2
0.742 0.280 19 40257052 stop gained C/A;T snv 1
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 2
rs137854567
APC
0.882 0.120 5 112819272 missense variant C/A;G;T snv 4.0E-06; 6.7E-04 1
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 4
rs121913341
BRAF
0.851 0.280 7 140753350 missense variant A/C;T snv 2
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 2
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 1
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 1
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 1
rs121913361
BRAF
0.807 0.280 7 140753349 missense variant C/A;G;T snv 1
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 1
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 1
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 1
rs121913375
BRAF
0.851 0.240 7 140753339 missense variant G/A;C snv 1
rs45580035
BRCA2
0.790 0.240 13 32380043 missense variant C/T snv 1.2E-05 1
rs80359204
BRCA2
1.000 0.040 13 32394741 missense variant A/G snv 1
rs104894340
CDK4
0.827 0.200 12 57751647 missense variant C/A;T snv 1
rs11547328
CDK4
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 1
rs104894094
CDKN2A
0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06 2
rs1064794292
CDKN2A
0.882 0.200 9 21974760 missense variant C/T snv 2
rs104894095
CDKN2A
0.827 0.120 9 21971200 missense variant C/G;T snv 9.0E-06 1