Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35502531
MLH1
0.827 0.160 3 37047639 missense variant AA/GC mnv 8
rs63750451
PMS2
0.827 0.160 7 5986883 stop gained G/A;C snv 1.6E-05 7
rs63751194
MLH1
0.851 0.160 3 37017508 missense variant C/A;T snv 4.0E-06 7
rs1418586322
MLH1
0.827 0.160 3 37050495 missense variant C/G snv 4.0E-06 6
rs143277125
PMS2
0.851 0.160 7 5992012 stop gained G/A;T snv 4.0E-06 6
rs63749939
MLH1
0.851 0.160 3 36996702 missense variant G/A snv 6
rs63750138
MSH6 ; FBXO11
0.851 0.160 2 47800297 missense variant C/A;G;T snv 2.0E-05; 8.0E-06 6
rs63750193
MLH1
0.851 0.160 3 37040276 missense variant T/C 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
rs267607845
MLH1
0.925 0.160 3 37042267 splice acceptor variant G/A;T snv 5
rs267607901
MLH1
0.882 0.160 3 37050633 frameshift variant AA/-;A;AAAA delins 5
rs267608078
FBXO11 ; MSH6
0.882 0.160 2 47803501 frameshift variant C/-;CC;CCC delins 5
rs63749873
MSH6 ; FBXO11
0.882 0.160 2 47795903 stop gained C/G snv 4.0E-06 1.4E-05 5
rs63749932
MSH2
0.882 0.160 2 47476399 stop gained C/G;T snv 1.6E-05; 4.0E-06 5
rs63750114
MLH1
0.827 0.160 3 37049015 stop gained C/A;T snv 4.9E-04 5
rs63750211
MLH1
0.882 0.160 3 37008904 missense variant A/G 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
rs63750575
MLH1
0.851 0.160 3 37047550 missense variant T/C snv 5
rs63750934
MSH2
0.882 0.160 2 47414368 stop gained C/T snv 5
rs63751094
MLH1
0.925 0.160 3 36996624 stop lost A/G;T snv 5
rs63751202
MLH1
0.851 0.160 3 37048578 missense variant T/C;G snv 5
rs63751428
MLH1
0.882 0.160 3 36996686 stop gained C/A;T snv 5