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: rs10993994
rs10993994
15 0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 0.800 1.000 37 2008 2020
dbSNP: rs1447295
rs1447295
29 0.658 0.400 8 127472793 intron variant A/C;T snv 0.800 0.914 35 2007 2019
dbSNP: rs6983267
rs6983267
62 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.800 0.871 31 2007 2019
dbSNP: rs16901979
rs16901979
17 0.724 0.480 8 127112671 intron variant C/A snv 0.16 0.800 0.955 22 2007 2019
dbSNP: rs4430796
rs4430796
14 0.790 0.280 17 37738049 intron variant A/G snv 0.52 0.800 1.000 21 2007 2019
dbSNP: rs2735839
rs2735839
7 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 0.800 0.938 16 2008 2019
dbSNP: rs137852578
rs137852578
AR
10 0.827 0.080 X 67723710 missense variant A/G snv 0.100 1.000 14 2002 2015
dbSNP: rs1859962
rs1859962
4 0.882 0.160 17 71112612 intron variant G/T snv 0.56 0.770 0.923 13 2007 2018
dbSNP: rs397507444
rs397507444
306 0.405 0.880 1 11794407 missense variant T/G snv 0.100 0.727 11 2004 2016
dbSNP: rs1056836
rs1056836
58 0.581 0.680 2 38071060 missense variant G/C snv 0.51 0.100 0.900 10 2000 2018
dbSNP: rs339331
rs339331
4 0.882 0.080 6 116888889 intron variant T/C snv 0.28 0.760 0.900 10 2010 2019
dbSNP: rs6983561
rs6983561
3 0.925 0.080 8 127094635 intron variant A/C snv 0.17 0.780 1.000 10 2008 2017
dbSNP: rs12653946
rs12653946
5 0.882 0.080 5 1895715 intron variant C/T snv 0.43 0.740 1.000 8 2010 2019
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: rs10090154
rs10090154
7 0.807 0.160 8 127519892 intergenic variant T/A;C snv 0.070 1.000 7 2008 2017
dbSNP: rs10486567
rs10486567
9 0.851 0.120 7 27936944 intron variant G/A snv 0.28 0.750 0.857 7 2010 2018
dbSNP: rs1800795
rs1800795
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.070 0.714 7 2009 2019
dbSNP: rs7679673
rs7679673
28 0.677 0.440 4 105140377 intron variant C/A snv 0.50 0.720 0.857 7 2009 2018
dbSNP: rs1131691014
rs1131691014
214 0.439 0.800 17 7676154 frameshift variant -/C ins 0.060 0.667 6 2007 2016
dbSNP: rs1512268
rs1512268
6 0.851 0.160 8 23668950 intergenic variant T/C snv 0.50 0.710 1.000 6 2009 2019
dbSNP: rs3787016
rs3787016
24 0.677 0.280 19 1090804 intron variant A/G snv 0.78 0.060 1.000 6 2011 2019
dbSNP: rs4242382
rs4242382
9 0.763 0.240 8 127505328 intergenic variant A/G;T snv 0.740 1.000 6 2008 2015
dbSNP: rs878854066
rs878854066
213 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.060 0.667 6 2007 2016
dbSNP: rs11649743
rs11649743
2 0.925 0.080 17 37714971 intron variant A/G snv 0.85 0.730 1.000 5 2011 2019
dbSNP: rs137852569
rs137852569
AR
10 0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 0.050 0.600 5 2001 2011