Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909237
PTEN
1.000 0.040 10 87933121 missense variant C/G snv 1
rs201613442
TNNI3K ; FPGT-TNNI3K ; LRRC53
1.000 0.040 1 74540276 missense variant G/A snv 4.0E-06 1
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 1
rs121913386
CDKN2A
0.807 0.120 9 21971018 missense variant G/A;T snv 1
rs397514495
TP53
0.882 0.120 17 7675070 missense variant C/A;T snv 1.2E-05 1
rs587782144
TP53
0.807 0.160 17 7675139 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 1
rs1057519922
NFE2L2
0.790 0.200 2 177234082 missense variant C/G;T snv 1
rs121913399
CTNNB1
0.724 0.200 3 41224612 missense variant G/A;C snv 1
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 2
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 1
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
rs28931589
CTNNB1
0.695 0.240 3 41224613 missense variant G/A;C;T snv 1
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 1
rs786203071
TP53
0.776 0.240 17 7675181 missense variant T/A;G snv 1
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 2
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 1
rs121434498
MAP2K2
0.807 0.280 19 4117553 missense variant A/C;G;T snv 1
rs267606870
IDH2
0.763 0.280 15 90088703 missense variant G/A;C snv 1
rs587777790
PIK3CA
0.732 0.280 3 179199690 missense variant G/A 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