Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750193
MLH1
0.851 0.160 3 37040276 missense variant T/C snv 3
rs63750206
MLH1
0.807 0.200 3 36996701 missense variant G/A;C;T snv 3
rs876658862
PMS2
0.925 0.160 7 5987567 stop gained G/A snv 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
rs146421227
MSH2
0.882 0.160 2 47482912 missense variant T/A snv 7.0E-06 2
rs587778914
MLH1
0.925 0.160 3 36996645 missense variant A/C snv 2
rs587779139
MSH2
0.925 0.160 2 47476513 stop gained C/G;T 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
rs63751192
MSH2
0.925 0.160 2 47429878 frameshift variant -/CGAC delins 2
rs63751236
MSH2
0.882 0.160 2 47475064 missense variant C/G;T snv 2
rs63751624
MSH2
0.925 0.160 2 47480871 missense variant G/A;C snv 2
rs864622258
MLH1
0.925 0.160 3 37050610 missense variant T/G snv 1.4E-05 2
rs876661116
PMS2
0.925 0.160 7 5977598 missense variant C/A;T snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs63751194
MLH1
0.851 0.160 3 37017508 missense variant C/A;T snv 4.0E-06 3
rs869312801
PMS2
0.882 0.160 7 5987062 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 4
rs1392665848
MLH1
0.925 0.160 3 37025865 missense variant A/G snv 4.0E-06 2
rs876659729
PMS2
0.925 0.160 7 5989828 synonymous variant G/A snv 4.0E-06 1.4E-05 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs786201226
MLH1
0.925 0.160 3 37014450 synonymous variant A/G;T snv 4.0E-06 2