Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs770167074
BMP2K
1.000 0.080 4 78826060 missense variant G/A;C snv 1.6E-05; 4.0E-06 1
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 1
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 1
rs121913386
CDKN2A
0.807 0.120 9 21971018 missense variant G/A;T snv 1
rs374711533
DCLK3
1.000 0.080 3 36718103 missense variant G/A snv 9.2E-05 1.6E-04 1
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 1
rs121918499
FGFR2
0.925 0.160 10 121520048 missense variant C/A;G snv 1
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 1
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 1
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 1
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 1
rs1057519922
NFE2L2
0.790 0.200 2 177234082 missense variant C/G;T snv 1
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
rs121913281
PIK3CA
0.623 0.520 3 179234296 missense variant C/T snv 1
rs587777790
PIK3CA
0.732 0.280 3 179199690 missense variant G/A snv 1
rs772110575
PIK3CA
0.807 0.160 3 179198938 missense variant G/A;T snv 4.0E-06 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
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 1
rs121918465
PTPN11
0.827 0.200 12 112450407 missense variant A/C;G;T snv 1
rs397507546
PTPN11
0.790 0.360 12 112489084 missense variant G/A;C;T 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