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: rs9332970
rs9332970
AR
1 1.000 0.160 X 67722905 missense variant T/C snv 0.700 1.000 20 1992 2004
dbSNP: rs9332971
rs9332971
AR
1 0.851 0.200 X 67722944 missense variant G/A;T snv 0.810 0.952 20 1992 2004
dbSNP: rs864622007
rs864622007
AR
2 0.882 0.200 X 67711621 missense variant T/A snv 0.700 0
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: rs137852589
rs137852589
AR
2 0.925 0.160 X 67721857 missense variant G/A;T snv 5.5E-06 0.800 1.000 20 1992 2004
dbSNP: rs137852598
rs137852598
AR
1 1.000 0.160 X 67722948 missense variant C/G;T snv 5.5E-06 0.800 1.000 20 1992 2004
dbSNP: rs754201976
rs754201976
AR
2 0.925 0.160 X 67686088 missense variant G/A snv 5.5E-06 0.800 1.000 20 1992 2004
dbSNP: rs886041133
rs886041133
AR
2 0.882 0.200 X 67723746 missense variant G/A;C snv 5.5E-06 0.800 1.000 20 1992 2014
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: rs773996740
rs773996740
AR
1 1.000 0.160 X 67546321 missense variant C/G;T snv 1.4E-05 0.700 0
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: 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: 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