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
7 0.878 0.071 X 67723710 missense variant A/G snp 0.900 0.917 22 1991 2015
dbSNP: rs864622007
rs864622007
AR
4 0.878 0.179 X 67711621 missense variant T/A snp 0.830 1.000 4 2002 2016
dbSNP: rs137852581
rs137852581
AR
3 0.923 0.071 X 67723701 missense variant C/T snp 0.820 0.500 3 1995 2007
dbSNP: rs137852571
rs137852571
AR
3 0.923 0.071 X 67717495 missense variant G/A snp 7.7E-05 0.810 1.000 6 1992 2004
dbSNP: rs138213197
rs138213197
15 0.744 0.179 17 48728343 missense variant C/T snp 1.8E-03 2.2E-03 0.800 0.870 25 2012 2017
dbSNP: rs137852580
rs137852580
AR
1 1.000 0.071 X 67723711 missense variant C/G snp 0.800 2 1985 1995
dbSNP: rs137852582
rs137852582
AR
1 1.000 0.071 X 67723786 missense variant A/G snp 0.800 1 1995 1995
dbSNP: rs137852583
rs137852583
AR
1 1.000 0.071 X 67711680 missense variant G/A snp 0.800 1 1995 1995
dbSNP: rs137852584
rs137852584
AR
1 1.000 0.071 X 67711459 missense variant G/A snp 0.800 1 1995 1995
dbSNP: rs137852603
rs137852603
1 1.000 0.071 10 110280017 missense variant A/C snp 0.800 1 1995 1995
dbSNP: rs351855
rs351855
35 0.642 0.357 5 177093242 missense variant G/A snp 0.33 0.27 0.760 1.000 11 2002 2016
dbSNP: rs1447295
rs1447295
9 0.801 0.107 8 127472793 intron variant A/C,T snp 0.82; 3.2E-05 0.760 1.000 7 2009 2013
dbSNP: rs137852593
rs137852593
AR
6 0.821 0.143 X 67717484 missense variant G/A,C,T snp 2.2E-05; 1.1E-05; 9.1E-04 1.4E-03 0.740 1.000 5 1996 2004
dbSNP: rs16901979
rs16901979
3 0.923 0.071 8 127112671 intron variant C/A snp 0.15 0.730 1.000 4 2009 2013
dbSNP: rs12653946
rs12653946
3 0.878 0.071 5 1895715 intron variant C/T snp 0.41 0.720 1.000 3 2012 2013
dbSNP: rs1456315
rs1456315
4 0.846 0.107 8 127091692 non coding transcript exon variant T/A,C snp 0.59 0.720 1.000 3 2011 2015
dbSNP: rs10896449
rs10896449
3 0.923 0.071 11 69227200 intergenic variant A/G snp 0.52 0.710 1.000 2 2009 2013
dbSNP: rs4242382
rs4242382
5 0.846 0.071 8 127505328 intergenic variant A/G,T snp 0.82 0.710 1.000 2 2013 2015
dbSNP: rs80358814
rs80358814
11 0.784 0.393 13 32340212 stop gained G/T snp 8.0E-06 0.710 1.000 2 2013 2015
dbSNP: rs137853009
rs137853009
3 0.878 0.107 22 28725030 missense variant C/A,T snp 4.0E-06; 6.0E-05 9.6E-05 0.700 3 2003 2005
dbSNP: rs35882952
rs35882952
2 1.000 0.071 1 22863060 missense variant G/C,T snp 4.0E-06; 1.1E-03 3.7E-03 0.700 3 2004 2007
dbSNP: rs77130927
rs77130927
1 1.000 0.071 22 28725031 missense variant G/A snp 1.0E-03 5.1E-04 0.700 2 2003 2014
dbSNP: rs1016343
rs1016343
3 0.923 0.071 8 127081052 non coding transcript exon variant C/T snp 0.21 0.700 1 2013 2013
dbSNP: rs10505477
rs10505477
12 0.744 0.179 8 127395198 intron variant A/G snp 0.41 0.700 1 2013 2013
dbSNP: rs111584802
rs111584802
1 1.000 0.071 5 75587055 missense variant A/G snp 0.700 1 2016 2016