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: rs10009409
rs10009409
1 1.000 0.080 4 72989536 intergenic variant C/T snv 0.35 0.700 1.000 2 2014 2018
dbSNP: rs1001179
rs1001179
CAT
33 0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 0.010 1.000 1 2016 2016
dbSNP: rs10012
rs10012
16 0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 0.020 1.000 2 2008 2015
dbSNP: rs1004030
rs1004030
1 1.000 0.080 14 22836440 upstream gene variant T/C snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs1004072779
rs1004072779
ERG
2 0.925 0.080 21 38403547 missense variant T/C snv 2.1E-05 0.010 1.000 1 2009 2009
dbSNP: rs10046
rs10046
18 0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 0.010 1.000 1 2010 2010
dbSNP: rs10069690
rs10069690
53 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2015 2015
dbSNP: rs10086908
rs10086908
1 1.000 0.080 8 126999692 intron variant T/C snv 0.28 0.700 1.000 2 2015 2019
dbSNP: rs10090154
rs10090154
7 0.807 0.160 8 127519892 intergenic variant T/A;C snv 0.070 1.000 7 2008 2017
dbSNP: rs1011970
rs1011970
22 0.677 0.320 9 22062135 intron variant G/T snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs10122495
rs10122495
1 1.000 0.080 9 34049781 upstream gene variant T/A snv 0.73 0.700 1.000 1 2018 2018
dbSNP: rs1012477
rs1012477
8 0.827 0.160 1 7798075 intron variant G/C snv 0.16 0.010 1.000 1 2009 2009
dbSNP: rs1016342
rs1016342
1 1.000 0.080 8 127080210 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2007 2007
dbSNP: rs1016343
rs1016343
8 0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 0.700 1.000 4 2007 2015
dbSNP: rs10165970
rs10165970
18 0.708 0.320 2 100840527 intron variant G/A snv 0.16 0.010 1.000 1 2017 2017
dbSNP: rs10175368
rs10175368
4 0.925 0.080 2 38080719 intron variant C/T snv 0.23 0.010 1.000 1 2018 2018
dbSNP: rs10187424
rs10187424
2 0.925 0.080 2 85567174 intron variant T/A;C snv 0.700 1.000 3 2011 2018
dbSNP: rs10194115
rs10194115
2 0.925 0.120 2 47012873 intron variant G/T snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs1024611
rs1024611
63 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2015 2015
dbSNP: rs1031588
rs1031588
1 1.000 0.080 8 127081032 non coding transcript exon variant C/A snv 0.24 0.700 1.000 1 2007 2007
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: rs1034528
rs1034528
5 0.882 0.120 1 11189075 intron variant G/C snv 0.30 0.010 1.000 1 2013 2013
dbSNP: rs1034866440
rs1034866440
AR
4 0.851 0.160 X 67643401 missense variant G/A snv 5.7E-06 0.050 0.600 5 2001 2011
dbSNP: rs1041258260
rs1041258260
2 0.925 0.080 19 43552170 missense variant C/T snv 8.0E-06 1.4E-05 0.010 1.000 1 2012 2012
dbSNP: rs1041449
rs1041449
1 1.000 0.080 21 41529494 intron variant A/G snv 0.42 0.700 1.000 1 2014 2014