Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 1
rs121434498
MAP2K2
0.807 0.280 19 4117553 missense variant A/C;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
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 1
rs371769427
U2AF1
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 1
rs34612342
MUTYH
0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 1
rs80338963
SMAD4
0.776 0.280 18 51065548 missense variant C/A;G;T snv 1
rs377767347
SMAD4
0.742 0.520 18 51065549 missense variant G/A;C;T snv 1
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 1
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 1
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 2
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 2
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 1
rs11554273
GNAS
0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 1
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 2
rs201613442
TNNI3K ; FPGT-TNNI3K ; LRRC53
1.000 0.040 1 74540276 missense variant G/A snv 4.0E-06 1
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 1
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 1
rs28934574
TP53
0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 1
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 1
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 1
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 1
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 1
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 1