Source: ALL
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
10 0.827 0.080 X 67723710 missense variant A/G snv 0.100 1.000 14 2002 2015
dbSNP: rs339331
rs339331
RFX6
4 0.882 0.080 6 116888889 intron variant T/C snv 0.28 0.760 0.900 10 2010 2019
dbSNP: rs6983561
rs6983561
PCAT1 ; CASC19
3 0.925 0.080 8 127094635 intron variant A/C snv 0.17 0.780 1.000 10 2008 2017
dbSNP: rs12653946
rs12653946
CTD-2194D22.4
5 0.882 0.080 5 1895715 intron variant C/T snv 0.43 0.740 1.000 8 2010 2019
dbSNP: rs627928
rs627928
RNASEL
10 0.790 0.080 1 182582202 missense variant A/C snv 0.54 0.49 0.080 0.875 8 2004 2019
dbSNP: rs17632542
rs17632542
KLK3
5 0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02 0.750 0.714 7 2011 2015
dbSNP: rs1902023
rs1902023
UGT2B15
4 0.882 0.080 4 68670366 missense variant A/C snv 0.51 0.53 0.070 0.857 7 2000 2017
dbSNP: rs11649743
rs11649743
HNF1B ; LOC105371754
2 0.925 0.080 17 37714971 intron variant A/G snv 0.85 0.730 1.000 5 2011 2019
dbSNP: rs266882
rs266882
KLK3
4 0.925 0.080 19 50854757 upstream gene variant G/A snv 0.49 0.050 0.800 5 2006 2018
dbSNP: rs149709822
rs149709822
KLK3
4 0.882 0.080 19 50856335 missense variant G/A snv 4.0E-05 2.3E-04 0.040 0.500 4 2001 2008
dbSNP: rs1983891
rs1983891
FOXP4
4 0.925 0.080 6 41568689 intron variant C/T snv 0.35 0.720 1.000 4 2010 2019
dbSNP: rs198977
rs198977
KLK2
4 0.925 0.080 19 50878521 missense variant C/T snv 0.24 0.30 0.040 1.000 4 2005 2015
dbSNP: rs9600079
rs9600079 		5 0.925 0.080 13 73154002 intergenic variant G/T snv 0.46 0.710 1.000 4 2010 2019
dbSNP: rs10187424
rs10187424
VAMP8
2 0.925 0.080 2 85567174 intron variant T/A;C snv 0.700 1.000 3 2011 2018
dbSNP: rs10875943
rs10875943 		2 0.925 0.080 12 49282227 intergenic variant T/A;C snv 0.700 1.000 3 2011 2018
dbSNP: rs11672691
rs11672691
PCAT19
3 0.925 0.080 19 41479679 non coding transcript exon variant G/A snv 0.42 0.720 0.667 3 2013 2018
dbSNP: rs11986220
rs11986220 		2 0.925 0.080 8 127519444 intergenic variant A/G;T snv 0.720 1.000 3 2009 2015
dbSNP: rs13385191
rs13385191
LDAH
4 0.925 0.080 2 20688505 intron variant A/G snv 0.20 0.720 1.000 3 2010 2014
dbSNP: rs16901966
rs16901966
PCAT1 ; CASC19
3 0.925 0.080 8 127098007 intron variant A/G snv 0.13 0.030 1.000 3 2012 2016
dbSNP: rs17599629
rs17599629
GOLPH3L
1 1.000 0.080 1 150685811 intron variant A/G snv 0.17 0.700 1.000 3 2014 2018
dbSNP: rs188140481
rs188140481
PCAT1 ; CASC19
4 0.925 0.080 8 127179427 non coding transcript exon variant T/A;C snv 0.720 1.000 3 2012 2015
dbSNP: rs2551188
rs2551188
CYP1B1 ; CYP1B1-AS1
2 0.925 0.080 2 38075651 non coding transcript exon variant C/T snv 0.35 0.030 1.000 3 2008 2019
dbSNP: rs620861
rs620861
POU5F1B ; CASC8 ; PCAT1 ; CASC21
3 0.925 0.080 8 127323428 intron variant G/A snv 0.36 0.030 0.667 3 2009 2017
dbSNP: rs636291
rs636291
PEX14
2 0.925 0.080 1 10496040 intron variant G/A snv 0.55 0.710 1.000 3 2014 2018
dbSNP: rs72552387
rs72552387
MSR1
3 0.882 0.080 8 16168568 missense variant C/A;G;T snv 1.6E-03; 4.0E-06 0.030 1.000 3 2003 2006