Source: BEFREE ×
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: rs5945619
rs5945619
LINC01496
2 0.882 0.160 X 51498820 non coding transcript exon variant C/T snv 0.720 1.000 2 2008 2018
dbSNP: rs61752561
rs61752561
KLK3
2 0.925 0.080 19 50858126 missense variant G/A snv 2.4E-02 2.5E-02 0.020 1.000 2 2010 2019
dbSNP: rs746367915
rs746367915
KLK3
2 0.925 0.080 19 50860089 missense variant C/T snv 8.0E-06 2.8E-05 0.020 1.000 2 2005 2010
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: rs1041258260
rs1041258260
XRCC1
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: rs10426628
rs10426628
SULT2B1
2 0.925 0.080 19 48589173 intron variant A/G snv 0.78 0.010 1.000 1 2014 2014
dbSNP: rs10459592
rs10459592
CYP19A1 ; MIR4713HG
2 0.925 0.080 15 51243944 intron variant T/G snv 0.49 0.010 1.000 1 2015 2015
dbSNP: rs1046040
rs1046040
POLR2E
2 0.925 0.080 19 1095515 upstream gene variant G/A snv 0.21 0.010 1.000 1 2019 2019
dbSNP: rs1057519966
rs1057519966
SPOP ; LOC107984999
2 0.882 0.080 17 49619064 missense variant A/C;T snv 0.010 1.000 1 2017 2017
dbSNP: rs1057519972
rs1057519972
SPOP ; LOC107984999
2 0.882 0.080 17 49619327 missense variant A/T snv 0.010 1.000 1 2017 2017
dbSNP: rs10740051
rs10740051
NCOA4
2 0.925 0.080 10 46025670 intron variant C/T snv 0.24 0.010 1.000 1 2011 2011
dbSNP: rs10749408
rs10749408 		2 0.925 0.080 10 121208012 intergenic variant C/T snv 0.72 0.010 1.000 1 2011 2011
dbSNP: rs10761581
rs10761581
NCOA4
2 0.925 0.080 10 46027444 missense variant A/C snv 0.44 0.41 0.010 1.000 1 2011 2011
dbSNP: rs10773338
rs10773338
LINC02405
2 0.925 0.080 12 126919857 intron variant G/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs10788165
rs10788165 		2 0.925 0.080 10 121284700 regulatory region variant T/G snv 0.35 0.010 1.000 1 2011 2011
dbSNP: rs10895304
rs10895304 		2 0.925 0.080 11 102519261 downstream gene variant A/G snv 0.20 0.010 1.000 1 2011 2011
dbSNP: rs10899221
rs10899221
EMSY
2 0.925 0.080 11 76470587 intron variant G/A;T snv 5.7E-02 0.010 1.000 1 2013 2013
dbSNP: rs10920531
rs10920531 		2 0.925 0.080 1 202939708 downstream gene variant A/C snv 0.57 0.010 1.000 1 2016 2016
dbSNP: rs10973794
rs10973794
IGFBPL1
2 0.925 0.080 9 38409359 intron variant G/A snv 0.15 0.010 1.000 1 2017 2017
dbSNP: rs10987883
rs10987883
SLC25A25-AS1
2 0.925 0.080 9 128118550 non coding transcript exon variant G/A snv 0.82 0.010 1.000 1 2011 2011
dbSNP: rs11063118
rs11063118
FGF23
2 0.925 0.080 12 4372398 intron variant T/C;G snv 0.010 1.000 1 2014 2014
dbSNP: rs11067228
rs11067228 		2 0.925 0.080 12 114656455 downstream gene variant A/G snv 0.37 0.010 1.000 1 2013 2013
dbSNP: rs11079344
rs11079344 		2 0.925 0.080 17 58297122 downstream gene variant A/G snv 0.14 0.010 1.000 1 2011 2011
dbSNP: rs11102001
rs11102001
GSTM5 ; EPS8L3
2 0.925 0.080 1 109757069 missense variant G/A snv 9.4E-02 0.16 0.010 1.000 1 2009 2009
dbSNP: rs11168314
rs11168314
VDR
2 0.925 0.080 12 47936846 intron variant G/A snv 0.23 0.010 1.000 1 2010 2010