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
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
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
rs864622007
AR
0.882 0.200 X 67711621 missense variant T/A snv 2
rs886041133
AR
0.882 0.200 X 67723746 missense variant G/A;C snv 5.5E-06 2
rs1057521122
AR
1.000 0.160 X 67722881 missense variant A/G snv 1
rs1254203917
AR
1.000 0.160 X 67721881 missense variant G/T snv 5.5E-06 1
rs1355285524
AR
1.000 0.160 X 67546480 missense variant A/G snv 1.8E-05 1.0E-05 1
rs137852562
AR
0.925 0.160 X 67721837 missense variant C/T snv 1
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 1
rs137852570
AR
1.000 0.160 X 67721876 missense variant A/G snv 1
rs137852577
AR
0.882 0.200 X 67722898 missense variant C/T snv 1
rs137852579
AR
1.000 0.160 X 67711549 missense variant T/C snv 1
rs137852585
AR
1.000 0.160 X 67711639 missense variant T/G snv 1
rs137852586
AR
1.000 0.160 X 67643378 missense variant G/A;T snv 1
rs137852587
AR
0.925 0.160 X 67643387 missense variant T/A snv 1
rs137852588
AR
0.925 0.160 X 67643284 missense variant C/T snv 1
rs137852595
AR
0.925 0.160 X 67711653 missense variant C/A;T snv 1
rs137852597
AR
1.000 0.160 X 67722973 missense variant T/C snv 1
rs137852598
AR
1.000 0.160 X 67722948 missense variant C/G;T snv 5.5E-06 1