Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17224367
MSH2
0.882 0.160 2 47429833 missense variant C/G;T snv 1.5E-03 2
rs63750492
MSH2
0.925 0.160 2 47466663 missense variant G/T snv 2
rs63750716
MSH2
0.925 0.160 2 47410232 missense variant A/G snv 4.7E-04 1.3E-04 2
rs1085308057
MSH2
0.925 0.160 2 47475244 missense variant A/G snv 1
rs1371291280
MSH2
1.000 0.160 2 47466702 missense variant T/A;C snv 4.0E-06 1
rs146421227
MSH2
0.882 0.160 2 47482912 missense variant T/A snv 7.0E-06 1
rs1553350676
MSH2
1.000 0.160 2 47410143 missense variant A/G snv 1
rs17217772
MSH2
0.790 0.240 2 47410107 missense variant A/C;G;T snv 5.8E-03 1
rs193922373
MSH2
1.000 0.160 2 47408493 missense variant G/A snv 2.4E-05 1
rs201118107
MSH2
1.000 0.160 2 47471051 missense variant A/C;G;T snv 8.0E-06; 1.0E-04; 1.2E-05 1
rs267607938
MSH2
1.000 0.160 2 47416344 missense variant A/G snv 8.0E-06 2.8E-05 1
rs267607959
MSH2
1.000 0.160 2 47463053 missense variant T/A;C snv 4.0E-06 1
rs267607980
MSH2
1.000 0.160 2 47475093 missense variant C/A;T snv 1
rs267607981
MSH2
1.000 0.160 2 47475177 missense variant A/G snv 1
rs267607982
MSH2
1.000 0.160 2 47475198 stop gained C/G;T snv 1.2E-05 1
rs267607994
MSH2
0.925 0.160 2 47476448 missense variant C/T snv 1
rs267607996
MSH2
0.925 0.160 2 47476382 missense variant G/A;C snv 1
rs267608007
MSH2
1.000 0.160 2 47478303 missense variant G/A;C;T snv 1
rs267608016
MSH2
1.000 0.160 2 47480754 missense variant T/A snv 8.0E-06 2.8E-05 1
rs267608022
MSH2
0.925 0.200 2 47482858 missense variant C/G;T snv 8.0E-06; 8.4E-05 1
rs267608023
MSH2
1.000 0.160 2 47482936 missense variant A/C snv 1
rs28929483
MSH2
0.925 0.160 2 47475130 missense variant C/A;G;T snv 1
rs28929484
MSH2
0.925 0.160 2 47475180 missense variant C/T snv 1
rs33946261
MSH2
1.000 0.160 2 47403329 missense variant C/G;T snv 2.2E-04 1.8E-04 1
rs34136999
MSH2
1.000 0.160 2 47414291 missense variant C/T snv 3.0E-04 4.5E-04 1