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: rs137852578
rs137852578
AR
10 0.827 0.080 X 67723710 missense variant A/G snv 0.800 1.000 14 2002 2015
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: rs627928
rs627928
10 0.790 0.080 1 182582202 missense variant A/C snv 0.54 0.49 0.080 0.875 8 2004 2019
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: rs1902023
rs1902023
4 0.882 0.080 4 68670366 missense variant A/C snv 0.51 0.53 0.070 0.857 7 2000 2017
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: rs7837688
rs7837688
2 0.925 0.080 8 127527115 intergenic variant T/G snv 0.91 0.710 1.000 7 2007 2013
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: rs137852603
rs137852603
1 1.000 0.080 10 110280017 missense variant A/C snv 0.800 1.000 5 2008 2015
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: rs266882
rs266882
4 0.925 0.080 19 50854757 upstream gene variant G/A snv 0.49 0.050 0.800 5 2006 2018
dbSNP: rs587780194
rs587780194
1 1.000 0.080 22 28699866 missense variant T/A;C snv 1.6E-05 0.700 1.000 5 2008 2015
dbSNP: rs750984976
rs750984976
1 1.000 0.080 22 28699879 missense variant T/C;G snv 4.0E-06 0.700 1.000 5 2008 2015
dbSNP: rs149709822
rs149709822
4 0.882 0.080 19 50856335 missense variant G/A snv 4.0E-05 2.3E-04 0.040 0.750 4 2000 2008
dbSNP: rs198977
rs198977
4 0.925 0.080 19 50878521 missense variant C/T snv 0.24 0.30 0.040 1.000 4 2005 2015
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: rs1058205
rs1058205
3 0.925 0.080 19 50860142 3 prime UTR variant C/T snv 0.75 0.74 0.720 1.000 3 2008 2018
dbSNP: rs11649743
rs11649743
2 0.925 0.080 17 37714971 intron variant A/G snv 0.85 0.030 1.000 3 2011 2018
dbSNP: rs13385191
rs13385191
4 0.925 0.080 2 20688505 intron variant A/G snv 0.20 0.720 1.000 3 2010 2014
dbSNP: rs138983188
rs138983188
2 0.925 0.080 17 7674863 missense variant G/A;T snv 4.0E-06 0.030 1.000 3 2013 2016
dbSNP: rs1983891
rs1983891
4 0.925 0.080 6 41568689 intron variant C/T snv 0.35 0.720 1.000 3 2010 2016
dbSNP: rs2551188
rs2551188
2 0.925 0.080 2 38075651 non coding transcript exon variant C/T snv 0.35 0.030 1.000 3 2008 2019
dbSNP: rs3760511
rs3760511
2 0.925 0.080 17 37746322 upstream gene variant G/A;T snv 0.720 1.000 3 2008 2018
dbSNP: rs72552387
rs72552387
3 0.882 0.080 8 16168568 missense variant C/A;G;T snv 1.6E-03; 4.0E-06 0.030 1.000 3 2003 2006
dbSNP: rs780354238
rs780354238
4 0.925 0.080 8 42369855 missense variant A/G snv 4.4E-06 0.030 1.000 3 2005 2017