Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63751656
MSH2
0.925 0.160 2 47466807 stop gained A/C;G;T snv 2
rs1553350250
MSH2
1.000 0.160 2 47408543 stop gained T/G snv 1
rs1558466577
MSH2
1.000 0.160 2 47416368 stop gained C/T snv 1
rs587779294
FBXO11 ; MSH6
1.000 0.160 2 47806470 stop gained G/A;C;T snv 1
rs63750058
MSH2
1.000 0.160 2 47414282 stop gained C/A;T snv 1
rs63750832
FBXO11 ; MSH6
1.000 0.160 2 47800075 stop gained C/A;G;T snv 8.0E-06 1
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs63750875
MSH2
0.742 0.280 2 47475171 missense variant G/A;C snv 1.6E-05 15
rs17217772
MSH2
0.790 0.240 2 47410107 missense variant A/C;G;T snv 5.8E-03 10
rs63750193
MLH1
0.851 0.160 3 37040276 missense variant T/C snv 6
rs63750610
MLH1
0.851 0.240 3 37048563 missense variant C/G;T snv 6
rs63750617
FBXO11 ; MSH6
0.851 0.160 2 47803473 missense variant C/G;T snv 4.0E-06; 9.5E-05 6
rs63750624
MSH2
0.925 0.160 2 47410211 missense variant G/A snv 6
rs63750781
MLH1
0.851 0.160 3 37004444 missense variant C/G;T snv 4.0E-06 6
rs63751207
MSH2
0.851 0.240 2 47466718 missense variant G/A;C;T snv 8.0E-06 6
rs587779067
MSH2
0.882 0.200 2 47416399 missense variant C/G;T snv 5
rs63750398
MSH2
0.925 0.160 2 47476451 missense variant G/A;T snv 5
rs63750453
MLH1
0.882 0.160 3 37001051 missense variant G/A snv 5
rs63751202
MLH1
0.851 0.160 3 37048578 missense variant T/C;G snv 5
rs28929483
MSH2
0.925 0.160 2 47475130 missense variant C/A;G;T snv 4
rs587778998
MLH1
0.925 0.160 3 37000991 missense variant A/G snv 8.0E-06 4
rs587779163
MSH2
0.882 0.160 2 47410220 missense variant T/G snv 4
rs587781462
MSH6 ; FBXO11
0.882 0.200 2 47800283 missense variant C/A;G;T snv 1.6E-05 4
rs63750232
MSH2
0.925 0.160 2 47476435 missense variant G/A;C;T snv 4
rs63750648
EPM2AIP1 ; MLH1
0.882 0.160 3 36993602 missense variant A/T snv 4