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: rs1262199907
rs1262199907
AR
2 1.000 0.160 X 67685960 missense variant C/T snv 5.5E-06 9.5E-06 0.010 1.000 1 2008 2008
dbSNP: rs139524801
rs139524801
AR
3 0.925 0.160 X 67643283 missense variant G/A;T snv 1.8E-04 0.010 1.000 1 2008 2008
dbSNP: rs141425171
rs141425171
AR
3 1.000 0.160 X 67717574 missense variant A/G;T snv 2.2E-05; 5.5E-06 0.010 1.000 1 2001 2001
dbSNP: rs200390780
rs200390780
AR
2 1.000 0.160 X 67546570 missense variant C/T snv 1.5E-03 1.1E-03 0.010 1.000 1 2008 2008