Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs2854744
IGFBP3
0.695 0.520 7 45921476 intron variant G/T snv 0.48 20
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs5742612
LOC105369944 ; IGF1
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02 11
rs63751012
EPM2AIP1 ; MLH1
0.851 0.200 3 36993656 stop gained G/A;C;T snv 5
rs2665802
GH1 ; CSHL1 ; LOC112268204
0.925 0.120 17 63917670 intron variant A/G;T snv 0.32 4
rs786202497
CHEK2
0.882 0.200 22 28719423 frameshift variant C/- del 4
rs863224501
MUTYH
0.925 0.160 1 45331519 frameshift variant TCACGGACGGG/- delins 2.1E-05 4
rs1021631442
FBXO11 ; MSH6
0.882 0.200 2 47806279 missense variant G/A snv 3
rs1553368590
MSH2
0.882 0.200 2 47475097 missense variant T/A snv 3
rs1553413710
MSH6 ; FBXO11
0.882 0.200 2 47800325 missense variant C/T snv 3
rs864622607
MSH6 ; FBXO11
0.882 0.200 2 47803678 missense variant T/G snv 3
rs1198119472
GSTA1
0.925 0.120 6 52799190 synonymous variant A/G snv 7.0E-06 2
rs730881833
MUTYH
0.827 0.160 1 45332242 missense variant C/A;T snv 4.0E-06; 2.8E-05 6
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs267608022
MSH2
0.925 0.200 2 47482858 missense variant C/G;T snv 8.0E-06; 8.4E-05 2
rs1042821
MSH6
0.732 0.280 2 47783349 missense variant G/A;C;T snv 0.18; 8.6E-06 16
rs536562413
FBXO11 ; MSH6
0.732 0.240 2 47799934 missense variant A/G snv 1.2E-05 7.0E-06 15
rs768623239
GSTM1 ; GSTM2
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs529008617
MUTYH
0.851 0.160 1 45331529 missense variant G/A snv 7.2E-05 2.8E-05 7
rs35352891
MUTYH
0.827 0.200 1 45331729 missense variant G/A snv 3.8E-04 1.1E-04 5
rs8042919
TRPM7
0.851 0.160 15 50586433 missense variant G/A;T snv 8.5E-02 5
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799977
MLH1
0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28