Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137852564
AR
0.827 0.240 X 67722976 missense variant G/A;T snv 5
rs864622007
AR
0.882 0.200 X 67711621 missense variant T/A snv 5
rs9332969
AR
0.827 0.240 X 67722899 missense variant G/A;T snv 5
rs1386577803
AR
0.851 0.240 X 67722872 missense variant G/A snv 4
rs9332971
AR
0.851 0.200 X 67722944 missense variant G/A;T snv 4
rs137852577
AR
0.882 0.200 X 67722898 missense variant C/T snv 3
rs968098233
AR
0.882 0.200 X 67546162 missense variant T/C snv 3
rs1085307685
AR
0.925 0.160 X 67717552 missense variant A/G snv 2
rs112374098
AR
0.925 0.200 X 67545417 stop gained C/A;T snv 2
rs137852562
AR
0.925 0.160 X 67721837 missense variant C/T snv 2
rs137852572
AR
0.925 0.160 X 67721838 missense variant G/A snv 2
rs137852587
AR
0.925 0.160 X 67643387 missense variant T/A snv 2
rs137852588
AR
0.925 0.160 X 67643284 missense variant C/T snv 2
rs137852595
AR
0.925 0.160 X 67711653 missense variant C/A;T snv 2
rs137852600
AR
0.925 0.160 X 67717535 missense variant G/A;T snv 2
rs1410383824
AR
0.925 0.160 X 67546470 stop gained G/A;T snv 2
rs1555969553
AR
0.925 0.200 X 67545438 stop gained C/T snv 2
rs1555969684
AR
0.925 0.200 X 67545892 frameshift variant -/G delins 2
rs1555970004
AR
0.925 0.200 X 67546581 frameshift variant -/C delins 2
rs1555982894
AR
0.925 0.160 X 67643409 splice donor variant T/C snv 2
rs1555990470
AR
0.925 0.200 X 67686046 missense variant G/A snv 2
rs1555995822
AR
0.925 0.200 X 67711569 missense variant G/A snv 2
rs1555996810
AR
0.925 0.200 X 67717480 missense variant T/C snv 2
rs1555996863
AR
0.925 0.200 X 67717600 missense variant G/A snv 2
rs1555997580
AR
0.925 0.200 X 67721873 stop gained C/T snv 2