Source: UNIPROT ×
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 3
rs137852591
AR
0.851 0.200 X 67721909 missense variant C/G snv 1.4E-03 1.4E-03 3
rs1085307685
AR
0.925 0.160 X 67717552 missense variant A/G snv 2
rs137852567
AR
0.882 0.200 X 67717595 missense variant A/G snv 2
rs137852572
AR
0.925 0.160 X 67721838 missense variant G/A snv 2
rs137852573
AR
0.807 0.280 X 67686064 missense variant G/A snv 2
rs137852576
AR
0.827 0.240 X 67686067 missense variant G/A snv 2
rs137852589
AR
0.925 0.160 X 67721857 missense variant G/A;T snv 5.5E-06 2
rs137852600
AR
0.925 0.160 X 67717535 missense variant G/A;T snv 2
rs754201976
AR
0.925 0.160 X 67686088 missense variant G/A snv 5.5E-06 2
rs886041133
AR
0.882 0.200 X 67723746 missense variant G/A;C snv 5.5E-06 2
rs104894742
AR
1.000 0.160 X 67545150 missense variant G/A snv 1
rs1064793480
AR
1.000 0.160 X 67721934 missense variant G/A snv 1
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 1
rs137852574
AR
0.925 0.160 X 67723688 missense variant T/G snv 1
rs137852577
AR
0.882 0.200 X 67722898 missense variant C/T snv 1
rs137852587
AR
0.925 0.160 X 67643387 missense variant T/A snv 1
rs137852592
AR
0.925 0.160 X 67721937 missense variant T/C snv 1
rs137852595
AR
0.925 0.160 X 67711653 missense variant C/A;T snv 1
rs139524801
AR
0.925 0.160 X 67643283 missense variant G/A;T snv 1.8E-04 1
rs141425171
AR
1.000 0.160 X 67717574 missense variant A/G;T snv 2.2E-05; 5.5E-06 1
rs142280455
AR
1.000 0.160 X 67686033 missense variant A/G snv 3.1E-04 3.8E-04 1
rs143040492
AR
0.882 0.200 X 67723690 missense variant C/T snv 1.1E-05 9.6E-06 1
rs1555982864
AR
1.000 0.160 X 67643344 missense variant G/T snv 1
rs201934623
AR
0.925 0.160 X 67546320 missense variant C/T snv 4.5E-03 2.0E-03 1