Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs1060503115
PMS2
0.763 0.400 7 5978664 missense variant T/A;G snv 13
rs63750217
MLH1
0.807 0.240 3 37048955 missense variant G/A;C snv 10
rs63750206
MLH1
0.807 0.200 3 36996701 missense variant G/A;C;T snv 9
rs1057515572
PMS2
0.882 0.200 7 5987033 frameshift variant GC/ACT delins 8
rs63749795
MLH1
0.807 0.240 3 37028833 stop gained C/T snv 8
rs267608150
PMS2
0.851 0.320 7 5997388 stop gained AGGGGG/CTTCACAAC;CTTCACACACA;NNNNNNNNNNN delins 7
rs63749843
MSH6 ; FBXO11
0.827 0.240 2 47803449 stop gained C/A;G;T snv 7
rs63750899
MLH1
0.851 0.200 3 37048562 missense variant C/G;T snv 7
rs63751108
MSH2
0.827 0.240 2 47429881 stop gained C/T snv 7
rs267607720
MLH1
0.851 0.240 3 37000952 splice region variant C/G;T snv 6
rs267607768
MLH1
0.851 0.240 3 37011867 splice region variant G/A;C snv 6
rs267607940
MSH2
0.851 0.240 2 47416430 splice donor variant G/A;T snv 6
rs63749849
MSH2
0.851 0.240 2 47429812 stop gained C/T snv 6
rs63750508
MSH2
0.851 0.240 2 47475126 stop gained C/G;T snv 6
rs63750540
MLH1
0.851 0.240 3 37025979 stop gained A/T snv 6
rs63750610
MLH1
0.851 0.240 3 37048563 missense variant C/G;T snv 6
rs63750636
MSH2
0.851 0.240 2 47476492 stop gained C/T snv 7.0E-06 6
rs63751017
FBXO11 ; MSH6
0.851 0.240 2 47800714 stop gained C/A;T snv 1.4E-05 6
rs63751247
MLH1
0.882 0.200 3 37047632 inframe deletion AAG/- delins 5
rs876660943
FBXO11 ; MSH6
0.882 0.240 2 47806359 splice donor variant G/T snv 7.0E-06 5
rs1553647894
MLH1
0.882 0.200 3 37020309 splice acceptor variant G/A;C snv 4
rs267607735
MLH1
0.851 0.240 3 37001058 splice region variant G/A snv 4
rs267608160
PMS2
0.925 0.200 7 5977669 frameshift variant GAAG/- del 4