Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750741
FBXO11 ; MSH6
0.827 0.200 2 47799329 missense variant T/C snv 1.2E-05 8
rs786201042
MSH6
0.827 0.240 2 47783243 stop gained C/G;T snv 2.5E-05 7
rs2020912
MSH6 ; FBXO11
0.807 0.480 2 47800616 missense variant T/C;G snv 5.1E-03 7
rs63749843
MSH6 ; FBXO11
0.827 0.240 2 47803449 stop gained C/A;G;T snv 7
rs63749999
FBXO11 ; MSH6
0.851 0.240 2 47801086 stop gained C/T snv 1.2E-05 6
rs63750111
FBXO11 ; MSH6
0.882 0.200 2 47800914 stop gained C/A;G snv 6
rs63751017
FBXO11 ; MSH6
0.851 0.240 2 47800714 stop gained C/A;T snv 1.4E-05 6
rs876660943
FBXO11 ; MSH6
0.882 0.240 2 47806359 splice donor variant G/T snv 7.0E-06 5
rs267608059
MSH6 ; FBXO11
0.882 0.240 2 47801050 stop gained G/T snv 5
rs587781462
MSH6 ; FBXO11
0.882 0.200 2 47800283 missense variant C/A;G;T snv 1.6E-05 4
rs63750664
MSH6
0.882 0.200 2 47783292 missense variant C/A;T snv 4.1E-06; 9.4E-05 3
rs63749889
MSH6 ; FBXO11
0.925 0.120 2 47800685 missense variant G/A snv 2.4E-05 7.0E-06 2