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: rs1010
rs1010
2 1.000 0.036 2 85581859 3 prime UTR variant T/C,G snp 0.45; 2.9E-04 0.010 1.000 1 2010 2010
dbSNP: rs1024323
rs1024323
5 0.878 0.107 4 3004316 missense variant C/A,G,T snp 0.36 0.46 0.010 1.000 1 2012 2012
dbSNP: rs1041740
rs1041740
3 1.000 0.036 21 31667849 intron variant C/T snp 0.23 0.010 1.000 1 2012 2012
dbSNP: rs10423928
rs10423928
5 0.878 0.107 19 45679046 intron variant T/A snp 0.20 0.010 1.000 1 2016 2016
dbSNP: rs1042714
rs1042714
38 0.634 0.464 5 148826910 stop gained G/C,T snp 0.68 0.67 0.010 1.000 1 2007 2007
dbSNP: rs10432782
rs10432782
6 0.821 0.107 21 31664078 intron variant T/G snp 0.19 0.010 1.000 1 2012 2012
dbSNP: rs1043994
rs1043994
2 19 15192033 synonymous variant T/A,C snp 4.0E-06; 0.85 0.88 0.010 1.000 1 2016 2016
dbSNP: rs1044498
rs1044498
8 0.801 0.250 6 131851228 missense variant A/C,G snp 0.19 0.32 0.010 1.000 1 2013 2013
dbSNP: rs10478723
rs10478723
1 6 12295228 intron variant G/A snp 0.14 0.010 1.000 1 2009 2009
dbSNP: rs104894833
rs104894833
5 0.878 0.143 X 101403984 missense variant C/G snp 1.2E-04 4.5E-05 0.010 1.000 1 2018 2018
dbSNP: rs1050450
rs1050450
21 0.692 0.500 3 49357401 missense variant G/A snp 0.28 0.30 0.010 1.000 1 2012 2012
dbSNP: rs10507875
rs10507875
1 13 77943119 intron variant A/G snp 0.17 0.010 1.000 1 2009 2009
dbSNP: rs1052700
rs1052700
1 15 89665079 3 prime UTR variant A/T snp 0.26 0.010 1.000 1 2008 2008
dbSNP: rs10743980
rs10743980
5 0.878 0.179 12 12259861 intron variant T/A,C,G snp 3.2E-05; 0.54 0.010 1.000 1 2016 2016
dbSNP: rs10757274
rs10757274
8 0.821 0.071 9 22096056 intron variant A/G snp 0.41 0.010 1.000 1 2010 2010
dbSNP: rs10887800
rs10887800
7 0.846 0.179 10 88316086 intron variant A/G,T snp 0.46 0.010 1.000 1 2012 2012
dbSNP: rs11030119
rs11030119
2 11 27706555 intron variant G/A,T snp 0.28 0.010 1.000 1 2015 2015
dbSNP: rs11172113
rs11172113
6 0.878 0.071 12 57133500 intron variant T/C snp 0.41 0.010 1.000 1 2016 2016
dbSNP: rs11196288
rs11196288
2 1.000 0.071 10 113297684 intergenic variant A/G snp 5.9E-02 0.010 1.000 1 2016 2016
dbSNP: rs11237379
rs11237379
2 1.000 0.071 11 78074911 intron variant T/C snp 0.39 0.010 1.000 1 2017 2017
dbSNP: rs112735431
rs112735431
8 0.801 0.071 17 80385145 missense variant G/A,C snp 2.6E-04; 8.0E-06 6.4E-05 0.010 1.000 1 2016 2016
dbSNP: rs1130864
rs1130864
CRP
17 0.707 0.321 1 159713301 3 prime UTR variant G/A snp 0.26 0.010 1.000 1 2011 2011
dbSNP: rs11542041
rs11542041
19 0.707 0.357 19 44908690 missense variant C/T snp 6.4E-05 0.010 1.000 1 2016 2016
dbSNP: rs11628722
rs11628722
1 14 94464768 missense variant A/G snp 0.78 0.71 0.010 1.000 1 2009 2009
dbSNP: rs11739136
rs11739136
9 0.846 0.143 5 170383792 missense variant C/T snp 9.9E-02 8.1E-02 0.010 1.000 1 2005 2005