Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799977
MLH1
0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28
rs587778883
MLH1
0.807 0.200 3 37025648 frameshift variant A/- del 6
rs63750217
MLH1
0.807 0.240 3 37048955 missense variant G/A;C snv 4
rs63749795
MLH1
0.807 0.240 3 37028833 stop gained C/T snv 3
rs63750206
MLH1
0.807 0.200 3 36996701 missense variant G/A;C;T snv 3
rs35502531
MLH1
0.827 0.160 3 37047639 missense variant AA/GC mnv 7
rs1418586322
MLH1
0.827 0.160 3 37050495 missense variant C/G snv 4.0E-06 6
rs28930073
MLH1
0.827 0.200 3 37007004 missense variant G/C snv 2.1E-04 1.9E-04 5
rs63750114
MLH1
0.827 0.160 3 37049015 stop gained C/A;T snv 4.9E-04 4
rs63750575
MLH1
0.851 0.160 3 37047550 missense variant T/C snv 4
rs63750899
MLH1
0.851 0.200 3 37048562 missense variant C/G;T snv 4
rs63751202
MLH1
0.851 0.160 3 37048578 missense variant T/C;G snv 4
rs63750193
MLH1
0.851 0.160 3 37040276 missense variant T/C snv 3
rs63751194
MLH1
0.851 0.160 3 37017508 missense variant C/A;T snv 4.0E-06 3
rs63751310
MLH1
0.851 0.200 3 37048595 stop gained C/T snv 3
rs63749939
MLH1
0.851 0.160 3 36996702 missense variant G/A snv 2
rs63750781
MLH1
0.851 0.160 3 37004444 missense variant C/G;T snv 4.0E-06 1
rs63751615
MLH1
0.851 0.200 3 37012098 stop gained C/A;T snv 4.0E-06 1
rs587778937
MLH1
0.882 0.160 3 37040291 missense variant T/C;G snv 4
rs267607713
MLH1
0.882 0.160 3 36996623 splice acceptor variant G/C snv 3
rs587778992
MLH1
0.882 0.200 3 37050606 stop gained C/T snv 2
rs63749820
MLH1
0.882 0.200 3 37007046 stop gained C/T snv 2
rs63750211
MLH1
0.882 0.160 3 37008904 missense variant A/G snv 2
rs63750656
MLH1 ; EPM2AIP1
0.882 0.160 3 36993632 missense variant G/T snv 2
rs63750693
MLH1
0.882 0.160 3 37047652 missense variant T/A;C snv 2