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: rs1800562
rs1800562
175 0.463 0.714 6 26092913 missense variant G/A snp 3.3E-02 3.8E-02 0.020 1.000 2 2001 2007
dbSNP: rs4804803
rs4804803
8 0.784 0.214 19 7747847 intergenic variant A/G snp 0.25 0.020 1.000 2 2012 2016
dbSNP: rs11540654
rs11540654
117 0.492 0.679 17 7676040 missense variant C/A,G,T snp 4.8E-05 3.2E-05 0.010 1.000 1 2013 2013
dbSNP: rs12252
rs12252
6 0.878 0.071 11 320772 splice region variant A/G snp 0.13 0.13 0.010 1.000 1 2013 2013
dbSNP: rs12375841
rs12375841
2 1.000 0.071 9 4850141 intron variant T/C snp 0.34 0.010 1.000 1 2013 2013
dbSNP: rs12487066
rs12487066
2 1.000 0.071 3 106193283 intergenic variant T/C snp 0.28 0.010 1.000 1 2015 2015
dbSNP: rs12711521
rs12711521
6 0.821 0.179 1 11030859 missense variant C/A snp 0.74 0.64 0.010 < 0.001 1 2008 2008
dbSNP: rs12979860
rs12979860
47 0.608 0.500 19 39248147 intron variant C/T snp 0.38 0.010 1.000 1 2014 2014
dbSNP: rs16944
rs16944
30 0.652 0.464 2 112837290 regulatory region variant A/G snp 0.58 0.010 1.000 1 2016 2016
dbSNP: rs179363878
rs179363878
5 0.846 0.143 21 44286089 missense variant T/C snp 2.8E-05 0.010 1.000 1 2007 2007
dbSNP: rs179363879
rs179363879
5 0.846 0.143 21 44286092 missense variant T/C snp 0.010 1.000 1 2007 2007
dbSNP: rs1799864
rs1799864
39 0.626 0.536 3 46357717 missense variant G/A snp 0.13 0.12 0.010 1.000 1 2007 2007
dbSNP: rs1800477
rs1800477
4 0.878 0.250 18 63318540 missense variant C/T snp 1.8E-02 5.7E-03 0.010 1.000 1 2013 2013
dbSNP: rs1800629
rs1800629
TNF
69 0.549 0.786 6 31575254 intergenic variant G/A snp 0.12 0.15 0.010 1.000 1 2017 2017
dbSNP: rs1818879
rs1818879
2 1.000 0.071 7 22733108 regulatory region variant G/A,C snp 0.30 0.010 1.000 1 2016 2016
dbSNP: rs1990760
rs1990760
16 0.744 0.286 2 162267541 missense variant C/T snp 0.50 0.46 0.010 1.000 1 2017 2017
dbSNP: rs2287622
rs2287622
16 0.707 0.179 2 168973818 missense variant A/C,G,T snp 0.57 0.57 0.010 1.000 1 2017 2017
dbSNP: rs2596542
rs2596542
10 0.756 0.143 6 31398818 intergenic variant C/T snp 0.38 0.010 1.000 1 2014 2014
dbSNP: rs28934571
rs28934571
14 0.744 0.179 17 7674216 missense variant C/A,G snp 0.010 1.000 1 2012 2012
dbSNP: rs3136558
rs3136558
2 1.000 0.071 2 112833698 intron variant A/G snp 0.22 0.010 1.000 1 2016 2016
dbSNP: rs3775291
rs3775291
30 0.647 0.464 4 186082920 missense variant C/G,T snp 1.2E-04; 0.28 1.6E-04; 0.24 0.010 1.000 1 2012 2012
dbSNP: rs397516808
rs397516808
1 12 112446327 synonymous variant A/G snp 1.6E-05 0.010 1.000 1 2016 2016
dbSNP: rs4553808
rs4553808
5 0.878 0.107 2 203866282 intergenic variant A/G snp 0.16 0.010 1.000 1 2014 2014
dbSNP: rs72550870
rs72550870
3 0.923 0.107 1 11046609 missense variant T/C snp 2.1E-02 2.5E-02 0.010 < 0.001 1 2008 2008
dbSNP: rs738409
rs738409
55 0.590 0.536 22 43928847 missense variant C/G snp 0.28 0.22 0.010 1.000 1 2013 2013