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: rs864622007
rs864622007
AR
5 0.882 0.200 X 67711621 missense variant T/A snv 0.830 1.000 3 2002 2010
dbSNP: rs1447295
rs1447295
29 0.658 0.400 8 127472793 intron variant A/C;T snv 0.800 0.917 36 2007 2018
dbSNP: rs138213197
rs138213197
24 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 0.800 0.935 31 2012 2019
dbSNP: rs10993994
rs10993994
15 0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 0.800 1.000 30 2008 2019
dbSNP: rs6983267
rs6983267
62 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.800 0.857 28 2007 2017
dbSNP: rs16901979
rs16901979
17 0.724 0.480 8 127112671 intron variant C/A snv 0.16 0.800 0.950 20 2007 2018
dbSNP: rs4430796
rs4430796
14 0.790 0.280 17 37738049 intron variant A/G snv 0.52 0.800 1.000 18 2008 2018
dbSNP: rs137852578
rs137852578
AR
10 0.827 0.080 X 67723710 missense variant A/G snv 0.800 1.000 14 2002 2015
dbSNP: rs2735839
rs2735839
7 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 0.800 0.923 13 2008 2019
dbSNP: rs137852603
rs137852603
1 1.000 0.080 10 110280017 missense variant A/C snv 0.800 1.000 5 2008 2015
dbSNP: rs137852564
rs137852564
AR
5 0.827 0.240 X 67722976 missense variant G/A;T snv 0.800 0
dbSNP: rs351855
rs351855
58 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.780 0.900 10 2005 2017
dbSNP: rs6983561
rs6983561
3 0.925 0.080 8 127094635 intron variant A/C snv 0.17 0.780 1.000 9 2008 2017
dbSNP: rs1859962
rs1859962
4 0.882 0.160 17 71112612 intron variant G/T snv 0.56 0.770 0.900 10 2008 2016
dbSNP: rs339331
rs339331
4 0.882 0.080 6 116888889 intron variant T/C snv 0.28 0.760 0.857 7 2010 2016
dbSNP: rs17632542
rs17632542
5 0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02 0.750 0.667 6 2011 2015
dbSNP: rs4242382
rs4242382
9 0.763 0.240 8 127505328 intergenic variant A/G;T snv 0.740 1.000 8 2008 2015
dbSNP: rs7501939
rs7501939
12 0.776 0.280 17 37741165 intron variant C/T snv 0.41 0.740 1.000 8 2008 2018
dbSNP: rs12653946
rs12653946
5 0.882 0.080 5 1895715 intron variant C/T snv 0.43 0.740 1.000 7 2010 2013
dbSNP: rs137852593
rs137852593
AR
8 0.827 0.160 X 67717484 missense variant G/A;C;T snv 2.2E-05; 1.1E-05; 9.1E-04 0.740 1.000 4 2000 2004
dbSNP: rs16901966
rs16901966
3 0.925 0.080 8 127098007 intron variant A/G snv 0.13 0.730 1.000 5 2008 2016
dbSNP: rs5945572
rs5945572
3 0.882 0.160 X 51486831 downstream gene variant A/G snv 0.730 1.000 4 2008 2010
dbSNP: rs620861
rs620861
3 0.925 0.080 8 127323428 intron variant G/A snv 0.36 0.730 0.750 4 2008 2017
dbSNP: rs103294
rs103294
7 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 0.730 1.000 3 2012 2014
dbSNP: rs1456315
rs1456315
9 0.790 0.200 8 127091692 non coding transcript exon variant T/A;C snv 0.720 1.000 6 2010 2014