Source: BEFREE

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 7
rs1418586322
MLH1
0.827 0.160 3 37050495 missense variant C/G snv 4.0E-06 6
rs587778937
MLH1
0.882 0.160 3 37040291 missense variant T/C;G snv 4
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
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
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
rs780406337
MLH1
1.000 0.160 3 37048919 missense variant G/C snv 4.0E-06 3
rs1060504000
MLH1
0.925 0.160 3 37025666 missense variant T/C snv 2
rs1260021106
MLH1
0.925 0.160 3 37025645 missense variant A/G snv 1.6E-05 2
rs1392665848
MLH1
0.925 0.160 3 37025865 missense variant A/G snv 4.0E-06 2
rs587778914
MLH1
0.925 0.160 3 36996645 missense variant A/C snv 2
rs63749818
MLH1
0.925 0.160 3 37007002 stop gained C/A;G;T snv 2
rs63749939
MLH1
0.851 0.160 3 36996702 missense variant G/A 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
rs63750791
MLH1
0.925 0.160 3 37025864 synonymous variant C/T snv 1.8E-04 2.1E-05 2
rs786201226
MLH1
0.925 0.160 3 37014450 synonymous variant A/G;T snv 4.0E-06 2
rs864622258
MLH1
0.925 0.160 3 37050610 missense variant T/G snv 1.4E-05 2
rs267607906
MLH1
1.000 0.160 3 37050576 stop gained A/C;G;T snv 1