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
rs63750114
MLH1
0.827 0.160 3 37049015 stop gained C/A;T snv 4.9E-04 4
rs28930073
MLH1
0.827 0.200 3 37007004 missense variant G/C snv 2.1E-04 1.9E-04 5
rs41295284
MLH1
0.925 0.160 3 37047607 missense variant T/A snv 1.9E-04 1.5E-04 1
rs63750791
MLH1
0.925 0.160 3 37025864 synonymous variant C/T snv 1.8E-04 2.1E-05 2
rs35045067
MLH1
0.925 0.160 3 37048557 missense variant A/C;G snv 4.4E-05 1
rs41295282
MLH1
1.000 0.160 3 37001024 missense variant A/G snv 1.6E-05 7.0E-05 1
rs63751615
MLH1
0.851 0.200 3 37012098 stop gained C/A;T snv 4.0E-06 1
rs1418586322
MLH1
0.827 0.160 3 37050495 missense variant C/G snv 4.0E-06 6
rs786201226
MLH1
0.925 0.160 3 37014450 synonymous variant A/G;T snv 4.0E-06 2
rs780406337
MLH1
1.000 0.160 3 37048919 missense variant G/C snv 4.0E-06 3
rs1392665848
MLH1
0.925 0.160 3 37025865 missense variant A/G snv 4.0E-06 2
rs63750781
MLH1
0.851 0.160 3 37004444 missense variant C/G;T snv 4.0E-06 1
rs63751194
MLH1
0.851 0.160 3 37017508 missense variant C/A;T snv 4.0E-06 3
rs35502531
MLH1
0.827 0.160 3 37047639 missense variant AA/GC mnv 7
rs587778883
MLH1
0.807 0.200 3 37025648 frameshift variant A/- del 6
rs587778937
MLH1
0.882 0.160 3 37040291 missense variant T/C;G snv 4
rs63750217
MLH1
0.807 0.240 3 37048955 missense variant G/A;C snv 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
rs267607713
MLH1
0.882 0.160 3 36996623 splice acceptor variant G/C snv 3
rs376642306
MLH1
0.925 0.160 3 37028819 missense variant T/C snv 3
rs587778966
MLH1
0.925 0.160 3 36996698 frameshift variant -/C delins 3
rs63749795
MLH1
0.807 0.240 3 37028833 stop gained C/T snv 3