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: rs113488022
rs113488022
267 0.407 0.786 7 140753336 missense variant snp 4.0E-06 0.100 0.800 10 2010 2016
dbSNP: rs121913529
rs121913529
70 0.559 0.393 12 25245350 missense variant C/A,G,T snp 4.0E-06 0.020 1.000 2 2011 2014
dbSNP: rs351855
rs351855
35 0.642 0.357 5 177093242 missense variant G/A snp 0.33 0.27 0.020 1.000 2 2004 2016
dbSNP: rs752021744
rs752021744
21 0.699 0.429 3 138759306 T/C snp 1.2E-05 0.020 1.000 2 2011 2012
dbSNP: rs758272654
rs758272654
28 0.667 0.536 20 58909201 synonymous variant T/C snp 4.0E-06 0.020 1.000 2 2006 2010
dbSNP: rs759728549
rs759728549
26 0.679 0.214 17 7676223 stop lost T/C snp 8.0E-06 0.020 1.000 2 2012 2014
dbSNP: rs104893626
rs104893626
8 0.846 0.214 2 136114915 stop gained G/C snp 0.010 1.000 1 2014 2014
dbSNP: rs11549465
rs11549465
27 0.662 0.357 14 61740839 missense variant C/T snp 8.8E-02 7.0E-02 0.010 1.000 1 2014 2014
dbSNP: rs11549467
rs11549467
14 0.734 0.250 14 61740857 missense variant G/A snp 8.9E-03 1.1E-02 0.010 1.000 1 2014 2014
dbSNP: rs11568818
rs11568818
7 0.801 0.179 11 102530930 regulatory region variant T/A,C snp 0.41 0.010 1.000 1 2015 2015
dbSNP: rs121434568
rs121434568
33 0.642 0.321 7 55191822 missense variant T/A,G snp 0.010 1.000 1 2013 2013
dbSNP: rs121434569
rs121434569
29 0.667 0.321 7 55181378 missense variant C/T snp 2.8E-05 9.6E-05 0.010 1.000 1 2016 2016
dbSNP: rs121912666
rs121912666
29 0.647 0.321 17 7674872 missense variant T/C,G snp 8.0E-06 0.010 1.000 1 2000 2000
dbSNP: rs137852578
rs137852578
AR
7 0.878 0.071 X 67723710 missense variant A/G snp 0.010 1.000 1 2002 2002
dbSNP: rs1695
rs1695
100 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2013 2013
dbSNP: rs17217772
rs17217772
8 0.784 0.214 2 47410107 missense variant A/G,T snp 5.8E-03 2.2E-02 0.010 1.000 1 2006 2006
dbSNP: rs1799782
rs1799782
84 0.523 0.607 19 43553422 stop gained G/A snp 9.5E-02 7.1E-02 0.010 1.000 1 2013 2013
dbSNP: rs193920817
rs193920817
2 1.000 0.107 17 7675131 missense variant C/T snp 0.010 1.000 1 2007 2007
dbSNP: rs2073778
rs2073778
1 22 20087052 non coding transcript exon variant C/T snp 0.14 0.010 1.000 1 2013 2013
dbSNP: rs2227983
rs2227983
12 0.734 0.214 7 55161562 stop gained G/A,C,T snp 0.29 0.23 0.010 < 0.001 1 2010 2010
dbSNP: rs25489
rs25489
48 0.587 0.571 19 43552260 stop lost C/G,T snp 8.5E-06; 7.1E-02 3.2E-05; 5.5E-02 0.010 1.000 1 2013 2013
dbSNP: rs3136797
rs3136797
5 0.923 0.071 8 42369287 missense variant C/G snp 1.1E-02 1.0E-02 0.010 1.000 1 2007 2007
dbSNP: rs37161548
rs37161548
2 1.000 None NA None 0.010 1.000 1 2014 2014
dbSNP: rs3761548
rs3761548
13 0.744 0.214 X 49261784 intron variant G/A,T snp 4.7E-05; 0.67; 1.4E-04 0.010 1.000 1 2014 2014
dbSNP: rs397514495
rs397514495
22 0.707 0.286 17 7675070 missense variant C/A,T snp 1.2E-05 3.2E-05 0.010 1.000 1 2012 2012