Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 1
rs11554273
GNAS
0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 1
rs121434498
MAP2K2
0.807 0.280 19 4117553 missense variant A/C;G;T 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
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 1
rs121912656
TP53
0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 1
rs121912657
TP53
0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 1
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 1
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G 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
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 1
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 1
rs121913385
CDKN2A
0.763 0.240 9 21971112 missense variant G/A;C snv 1
rs121913386
CDKN2A
0.807 0.120 9 21971018 missense variant G/A;T snv 1
rs121913399
CTNNB1
0.724 0.200 3 41224612 missense variant G/A;C snv 1
rs121913502
IDH2
0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 1
rs138729528
TP53
0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 1
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 1
rs201613442
TNNI3K ; FPGT-TNNI3K ; LRRC53
1.000 0.040 1 74540276 missense variant G/A snv 4.0E-06 1
rs267606870
IDH2
0.763 0.280 15 90088703 missense variant G/A;C snv 1