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: rs1045531
rs1045531
PSCA
3 0.882 0.080 8 142682129 synonymous variant C/A snv 0.45 0.44 0.020 1.000 2 2011 2017
dbSNP: rs10505483
rs10505483
PCAT1 ; CASC19
2 0.925 0.080 8 127112950 intron variant C/T snv 0.16 0.700 1.000 2 2008 2012
dbSNP: rs1057519864
rs1057519864
AR
8 0.851 0.080 X 67723707 missense variant T/C snv 0.020 1.000 2 2013 2015
dbSNP: rs10948059
rs10948059
GNMT ; CNPY3-GNMT
3 0.925 0.080 6 42960723 upstream gene variant C/G;T snv 0.39 0.020 1.000 2 2014 2016
dbSNP: rs11006207
rs11006207 		1 1.000 0.080 10 46057646 regulatory region variant A/G snv 0.45 0.700 1.000 2 2008 2008
dbSNP: rs11672691
rs11672691
PCAT19
3 0.925 0.080 19 41479679 non coding transcript exon variant G/A snv 0.42 0.720 0.500 2 2013 2018
dbSNP: rs11781886
rs11781886
NKX3-1 ; LOC107986930
2 0.925 0.080 8 23682904 5 prime UTR variant C/T snv 0.72 0.72 0.020 1.000 2 2010 2014
dbSNP: rs119484086
rs119484086
ELAC2
5 0.851 0.080 17 12992957 missense variant C/A;T snv 4.0E-06; 5.3E-04 0.020 1.000 2 2005 2019
dbSNP: rs11986220
rs11986220 		2 0.925 0.080 8 127519444 intergenic variant A/G;T snv 0.020 1.000 2 2009 2012
dbSNP: rs11988857
rs11988857 		1 1.000 0.080 8 127519628 intergenic variant G/A snv 0.80 0.700 1.000 2 2008 2008
dbSNP: rs12418451
rs12418451
LOC338694 ; LOC105369366
3 0.882 0.080 11 69167951 intron variant G/A snv 0.22 0.020 1.000 2 2009 2015
dbSNP: rs12757998
rs12757998 		3 0.925 0.080 1 182569343 downstream gene variant C/T snv 0.24 0.020 1.000 2 2010 2013
dbSNP: rs1353855643
rs1353855643
ELAC2
2 0.925 0.080 17 13000197 frameshift variant T/- del 4.0E-06 0.020 0.500 2 2005 2008
dbSNP: rs137852581
rs137852581
AR
5 0.882 0.080 X 67723701 missense variant C/T snv 0.720 1.000 2 1997 2007
dbSNP: rs1446725892
rs1446725892
ELAC2
2 0.925 0.080 17 13000197 missense variant T/C;G snv 4.0E-06; 8.0E-06 0.020 0.500 2 2005 2008
dbSNP: rs16901970
rs16901970
PCAT1 ; CASC19
1 1.000 0.080 8 127100470 intron variant T/G snv 0.13 0.700 1.000 2 2008 2012
dbSNP: rs17023900
rs17023900 		2 0.925 0.080 3 87085650 upstream gene variant A/G snv 7.1E-02 0.700 1.000 2 2008 2012
dbSNP: rs17036508
rs17036508
MTOR ; ANGPTL7
4 0.925 0.080 1 11195977 3 prime UTR variant T/C snv 9.0E-02 0.020 1.000 2 2013 2017
dbSNP: rs17884057
rs17884057
SOD1
2 0.925 0.080 21 31664502 intron variant AGA/- delins 0.13 0.020 1.000 2 2011 2013
dbSNP: rs188140481
rs188140481
PCAT1 ; CASC19
4 0.925 0.080 8 127179427 non coding transcript exon variant T/A;C snv 0.020 1.000 2 2015 2015
dbSNP: rs200331695
rs200331695
EMSY
2 0.925 0.080 11 76463778 intron variant A/G snv 8.0E-04 4.7E-04 0.020 1.000 2 2015 2016
dbSNP: rs2171492
rs2171492
CPA4
2 0.925 0.080 7 130310900 missense variant G/T snv 0.35 0.33 0.020 1.000 2 2009 2012
dbSNP: rs266849
rs266849
LOC105372441
4 0.925 0.080 19 50845834 intron variant G/A snv 0.82 0.710 1.000 2 2008 2012
dbSNP: rs3195676
rs3195676
AMACR ; C1QTNF3-AMACR
2 0.925 0.080 5 34007995 missense variant C/T snv 0.42 0.41 0.020 1.000 2 2007 2013
dbSNP: rs4054823
rs4054823 		3 0.882 0.080 17 13721707 intergenic variant T/C snv 0.42 0.020 1.000 2 2011 2012