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: rs121434592
rs121434592
56 0.582 0.500 14 104780214 missense variant C/T snp 4.0E-06 0.700 3 2012 2015
dbSNP: rs121913430
rs121913430
2 1.000 0.071 7 55174740 missense variant G/A snp 0.700 1 2015 2015
dbSNP: rs137852578
rs137852578
AR
7 0.878 0.071 X 67723710 missense variant A/G snp 0.020 0.500 2 2002 2012
dbSNP: rs138213197
rs138213197
15 0.744 0.179 17 48728343 missense variant C/T snp 1.8E-03 2.2E-03 0.020 1.000 2 2013 2017
dbSNP: rs1060501201
rs1060501201
3 0.923 0.071 17 7674190 missense variant T/C snp 0.010 1.000 1 2017 2017
dbSNP: rs113488022
rs113488022
267 0.407 0.786 7 140753336 missense variant snp 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs1197734477
rs1197734477
3 0.923 0.071 10 87961012 missense variant A/G snp 0.010 1.000 1 2017 2017
dbSNP: rs137852581
rs137852581
AR
3 0.923 0.071 X 67723701 missense variant C/T snp 0.010 1.000 1 2005 2005
dbSNP: rs140191758
rs140191758
3 0.923 0.071 11 128937724 stop gained G/A,C,T snp 3.2E-05; 4.0E-06; 6.9E-04 8.6E-04 0.010 1.000 1 2006 2006
dbSNP: rs1571801
rs1571801
3 0.923 0.071 9 121665094 intron variant G/T snp 0.22 0.010 1.000 1 2007 2007
dbSNP: rs16861209
rs16861209
1 3 186845325 intron variant C/A,G snp 9.3E-02 0.010 1.000 1 2012 2012
dbSNP: rs17366568
rs17366568
2 3 186852664 non coding transcript exon variant G/A snp 8.8E-02 0.010 1.000 1 2012 2012
dbSNP: rs182052
rs182052
9 0.801 0.250 3 186842993 intron variant G/A snp 0.39 0.010 1.000 1 2012 2012
dbSNP: rs266729
rs266729
21 0.679 0.429 3 186841685 intergenic variant C/A,G,T snp 6.4E-05; 0.23 0.010 1.000 1 2012 2012
dbSNP: rs28909982
rs28909982
3 0.923 0.071 22 28725338 missense variant T/C snp 1.2E-04 6.4E-05 0.010 1.000 1 2006 2006
dbSNP: rs339331
rs339331
4 0.878 0.071 6 116888889 intron variant T/C snp 0.30 0.010 1.000 1 2014 2014
dbSNP: rs368015309
rs368015309
6 0.821 0.107 9 78304929 missense variant G/A snp 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs375118292
rs375118292
3 0.923 0.071 2 224506080 missense variant T/A,C snp 2.0E-05 0.010 1.000 1 2014 2014
dbSNP: rs3774261
rs3774261
1 3 186853770 splice region variant A/G snp 0.57 0.010 1.000 1 2012 2012
dbSNP: rs486907
rs486907
16 0.715 0.286 1 182585422 missense variant C/T snp 0.31 0.30 0.010 1.000 1 2010 2010
dbSNP: rs587781710
rs587781710
1 22 28687938 stop gained C/A,G,T snp 4.3E-06; 2.1E-05 0.010 1.000 1 2006 2006
dbSNP: rs587782480
rs587782480
1 22 28699888 missense variant T/C snp 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs727502792
rs727502792
3 0.923 0.071 17 49601958 missense variant T/A snp 0.010 1.000 1 2014 2014
dbSNP: rs730881689
rs730881689
1 22 28696951 missense variant T/C,G snp 0.010 1.000 1 2006 2006
dbSNP: rs7639352
rs7639352
1 3 186860685 intergenic variant C/T snp 0.29 0.010 1.000 1 2012 2012