Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519922
NFE2L2
0.790 0.200 2 177234082 missense variant C/G;T snv 1
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 7
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 5
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 4
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
rs121913283
PIK3CA
0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 2
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 2
rs1057519925
PIK3CA
0.683 0.560 3 179210291 missense variant G/A;C snv 1
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 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
rs121913287
PIK3CA
0.752 0.400 3 179199088 missense variant G/A snv 1
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 1
rs587777790
PIK3CA
0.732 0.280 3 179199690 missense variant G/A snv 1
rs867262025
PIK3CA
0.790 0.360 3 179221146 missense variant G/A snv 1
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 1
rs121909237
PTEN
1.000 0.040 10 87933121 missense variant C/G snv 1
rs377767347
SMAD4
0.742 0.520 18 51065549 missense variant G/A;C;T snv 1
rs80338963
SMAD4
0.776 0.280 18 51065548 missense variant C/A;G;T snv 1
rs201613442
TNNI3K ; FPGT-TNNI3K ; LRRC53
1.000 0.040 1 74540276 missense variant G/A snv 4.0E-06 1
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 1
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 1
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 1
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 1