Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003158162
TTN-AS1 ; TTN
1.000 0.080 2 178531968 missense variant G/A snv 4.0E-06 1
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 4
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
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 1
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 2
rs104894231
LRRC56 ; HRAS
0.776 0.360 11 533467 missense variant C/G;T snv 1
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 1
rs1057519893
ERBB3
0.790 0.160 12 56085070 missense variant G/A;T snv 1
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;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
rs1057519945
POLE
0.776 0.200 12 132673703 missense variant C/A;T snv 1
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
rs11554273
GNAS
0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 1
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 4
rs121434498
MAP2K2
0.807 0.280 19 4117553 missense variant A/C;G;T snv 1
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 2
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 2
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 1
rs121912580
SMAD4
0.807 0.280 18 51067036 missense variant G/A;C;T 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