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: rs11154178
rs11154178
4 0.878 0.179 6 123540174 intron variant T/A,C snp 0.61; 3.2E-05 0.700 1 2017 2017
dbSNP: rs28485846
rs28485846
4 0.878 0.179 8 35265058 intron variant C/T snp 4.9E-02 0.700 1 2017 2017
dbSNP: rs28928910
rs28928910
10 0.846 0.107 8 24956452 missense variant G/A,T snp 0.700 1 2015 2015
dbSNP: rs3761980
rs3761980
4 0.878 0.179 6 36026129 intergenic variant A/G snp 0.14 0.700 1 2017 2017
dbSNP: rs71597855
rs71597855
4 0.878 0.179 4 53790270 G/A snp 2.9E-02 0.700 1 2017 2017
dbSNP: rs755919784
rs755919784
2 1.000 0.071 20 13072400 missense variant T/C snp 2.6E-05 3.2E-05 0.700 1 2016 2016
dbSNP: rs774909609
rs774909609
2 9 34990673 missense variant C/T snp 1.2E-04 1.6E-04 0.700 1 2016 2016
dbSNP: rs80028505
rs80028505
4 0.878 0.179 6 36030611 intron variant C/G,T snp 0.12 0.700 1 2017 2017
dbSNP: rs879253869
rs879253869
1 8 81444935 missense variant A/T snp 0.700 1 2016 2016
dbSNP: rs587783070
rs587783070
3 1.000 1 220143109 missense variant C/T snp 0.700 0
dbSNP: rs1695
rs1695
100 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.040 1.000 4 2006 2013
dbSNP: rs104894619
rs104894619
6 0.821 0.107 17 15231047 missense variant G/A snp 4.0E-03 5.3E-03 0.020 1.000 2 2006 2011
dbSNP: rs104894621
rs104894621
7 0.846 0.071 17 15239575 missense variant G/A snp 0.020 1.000 2 1998 1999
dbSNP: rs57105105
rs57105105
4 0.923 0.071 8 24953776 missense variant C/T snp 0.020 1.000 2 2004 2016
dbSNP: rs62636503
rs62636503
5 0.878 0.071 8 24953779 missense variant C/T snp 0.020 1.000 2 2004 2016
dbSNP: rs924607
rs924607
5 0.878 0.107 5 609978 intron variant C/T snp 0.34 0.020 1.000 2 2015 2016
dbSNP: rs1045642
rs1045642
108 0.520 0.714 7 87509329 synonymous variant A/G,T snp 0.50 0.56 0.010 1.000 1 2007 2007
dbSNP: rs104894075
rs104894075
5 0.846 0.071 8 74362940 stop gained C/G snp 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs104894077
rs104894077
5 0.878 0.071 8 74361886 stop gained C/T snp 7.6E-05 0.010 1.000 1 2010 2010
dbSNP: rs104894078
rs104894078
5 0.846 0.071 8 74360184 missense variant C/T snp 3.2E-05 0.010 1.000 1 2013 2013
dbSNP: rs104894707
rs104894707
PRX
3 0.923 0.071 19 40396207 stop gained A/T snp 8.0E-06 0.010 1.000 1 2002 2002
dbSNP: rs10636
rs10636
4 0.923 0.071 16 56609431 3 prime UTR variant G/C snp 0.26 0.010 1.000 1 2008 2008
dbSNP: rs11076161
rs11076161
2 1.000 0.071 16 56639236 intron variant A/G snp 0.71 0.67 0.010 1.000 1 2008 2008
dbSNP: rs1159057
rs1159057
1 4 65271097 intergenic variant C/T snp 0.34 0.010 1.000 1 2014 2014
dbSNP: rs116840817
rs116840817
3 0.923 0.071 X 71223852 missense variant T/C snp 0.010 1.000 1 2002 2002