Gene: AR ×
Source: UNIPROT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1555997625
rs1555997625
AR
1 1.000 0.160 X 67721951 missense variant C/T snv 0.710 1.000 20 1992 2004
dbSNP: rs1057521122
rs1057521122
AR
1 1.000 0.160 X 67722881 missense variant A/G snv 0.700 1.000 20 1992 2004
dbSNP: rs1085307685
rs1085307685
AR
2 0.925 0.160 X 67717552 missense variant A/G snv 0.700 1.000 20 1992 2004
dbSNP: rs1254203917
rs1254203917
AR
1 1.000 0.160 X 67721881 missense variant G/T snv 5.5E-06 0.700 1.000 20 1992 2004
dbSNP: rs1355285524
rs1355285524
AR
1 1.000 0.160 X 67546480 missense variant A/G snv 1.8E-05 1.0E-05 0.700 1.000 20 1992 2004
dbSNP: rs137852588
rs137852588
AR
1 0.925 0.160 X 67643284 missense variant C/T snv 0.700 1.000 20 1992 2004
dbSNP: rs137852591
rs137852591
AR
3 0.851 0.200 X 67721909 missense variant C/G snv 1.4E-03 1.4E-03 0.700 1.000 20 1992 2004
dbSNP: rs1555998105
rs1555998105
AR
1 1.000 0.160 X 67723774 missense variant T/C snv 0.700 1.000 20 1992 2004
dbSNP: rs201934623
rs201934623
AR
1 0.925 0.160 X 67546320 missense variant C/T snv 4.5E-03 2.0E-03 0.700 1.000 20 1992 2004
dbSNP: rs755226547
rs755226547
AR
1 1.000 0.160 X 67723737 missense variant A/G;T snv 1.3E-04; 5.5E-06 0.700 1.000 20 1992 2004
dbSNP: rs768869912
rs768869912
AR
1 1.000 0.160 X 67717488 missense variant C/G snv 1.1E-05 0.700 1.000 20 1992 2004
dbSNP: rs9332970
rs9332970
AR
1 1.000 0.160 X 67722905 missense variant T/C snv 0.700 1.000 20 1992 2004
dbSNP: rs773996740
rs773996740
AR
1 1.000 0.160 X 67546321 missense variant C/G;T snv 1.4E-05 0.700 0
dbSNP: rs864622007
rs864622007
AR
2 0.882 0.200 X 67711621 missense variant T/A snv 0.700 0