Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201934623
AR
0.925 0.160 X 67546320 missense variant C/T snv 4.5E-03 2.0E-03 2
rs200390780
AR
1.000 0.160 X 67546570 missense variant C/T snv 1.5E-03 1.1E-03 2
rs137852591
AR
0.851 0.200 X 67721909 missense variant C/G snv 1.4E-03 1.4E-03 4
rs139524801
AR
0.925 0.160 X 67643283 missense variant G/A;T snv 1.8E-04 3
rs755226547
AR
1.000 0.160 X 67723737 missense variant A/G;T snv 1.3E-04; 5.5E-06 1
rs370215797
AR
1.000 0.160 X 67545621 missense variant G/A snv 1.2E-04 1.3E-04 1
rs1199988820
AR
1.000 0.160 X 67545363 stop gained C/G;T snv 7.3E-05 1
rs766161615
AR
1.000 0.160 X 67546589 stop gained C/G;T snv 5.8E-05 9.8E-06 1
rs750324117
AR
1.000 0.160 X 67546011 stop gained G/A;T snv 2.2E-05 1
rs1355285524
AR
1.000 0.160 X 67546480 missense variant A/G snv 1.8E-05 1.0E-05 1
rs773996740
AR
1.000 0.160 X 67546321 missense variant C/G;T snv 1.4E-05 1
rs143040492
AR
0.882 0.200 X 67723690 missense variant C/T snv 1.1E-05 9.6E-06 3
rs768869912
AR
1.000 0.160 X 67717488 missense variant C/G snv 1.1E-05 1
rs137852563
AR
1.000 0.160 X 67711673 stop gained G/A snv 5.7E-06 1
rs1262199907
AR
1.000 0.160 X 67685960 missense variant C/T snv 5.5E-06 9.5E-06 2
rs754515125
AR
1.000 0.160 X 67722821 splice region variant C/A;G;T snv 5.5E-06 1
rs372903533
AR
0.925 0.200 X 67711599 missense variant C/T snv 5.5E-06 9.5E-06 2
rs886041133
AR
0.882 0.200 X 67723746 missense variant G/A;C snv 5.5E-06 3
rs754201976
AR
0.925 0.160 X 67686088 missense variant G/A snv 5.5E-06 2
rs137852598
AR
1.000 0.160 X 67722948 missense variant C/G;T snv 5.5E-06 1
rs137852565
AR
0.925 0.200 X 67721905 stop gained G/A;C snv 5.5E-06 2
rs137852589
AR
0.925 0.160 X 67721857 missense variant G/A;T snv 5.5E-06 2
rs1254203917
AR
1.000 0.160 X 67721881 missense variant G/T snv 5.5E-06 1
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 10
rs137852573
AR
0.807 0.280 X 67686064 missense variant G/A snv 6