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: rs1132358
rs1132358
3 1.000 0.036 16 1347814 synonymous variant C/T snp 0.44 0.38 0.010 1.000 1 2013 2013
dbSNP: rs1133503
rs1133503
5 0.923 0.036 6 95606712 3 prime UTR variant C/G,T snp 0.59 0.010 1.000 1 2015 2015
dbSNP: rs1202184
rs1202184
6 0.846 0.107 7 87584585 intron variant C/T snp 0.41 0.010 1.000 1 2011 2011
dbSNP: rs121912438
rs121912438
47 0.630 0.464 21 31667299 missense variant G/A,C snp 1.2E-05; 8.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs12454712
rs12454712
8 0.923 0.107 18 63178651 intron variant T/A,C snp 0.36 0.010 1.000 1 2010 2010
dbSNP: rs1360780
rs1360780
16 0.769 0.107 6 35639794 intron variant T/A,C snp 0.69 0.010 1.000 1 2014 2014
dbSNP: rs16139
rs16139
27 0.657 0.500 7 24285260 missense variant T/A,C snp 4.0E-06; 3.0E-02 3.2E-02 0.010 1.000 1 2009 2009
dbSNP: rs165599
rs165599
18 0.715 0.250 22 19969258 3 prime UTR variant G/A snp 0.57 0.010 1.000 1 2015 2015
dbSNP: rs1799964
rs1799964
15 0.724 0.429 6 31574531 intergenic variant T/C snp 0.19 0.010 1.000 1 2016 2016
dbSNP: rs1881457
rs1881457
7 0.801 0.214 5 132656717 intron variant A/C snp 0.22 0.010 < 0.001 1 2014 2014
dbSNP: rs1922242
rs1922242
5 0.878 0.071 7 87544351 intron variant A/T snp 0.43 0.010 1.000 1 2011 2011
dbSNP: rs1960264
rs1960264
2 1.000 0.036 X 23781758 intron variant C/G,T snp 0.66 0.010 1.000 1 2009 2009
dbSNP: rs2020936
rs2020936
6 0.821 0.071 17 30223796 intron variant G/A,C snp 0.76 0.010 1.000 1 2009 2009
dbSNP: rs2072115
rs2072115
4 0.878 0.071 12 47751585 intron variant A/C,G snp 3.2E-05; 0.23 0.010 1.000 1 2010 2010
dbSNP: rs2234693
rs2234693
50 0.590 0.571 6 151842200 intron variant T/C snp 0.47 0.010 1.000 1 2013 2013
dbSNP: rs2235632
rs2235632
3 1.000 0.036 16 1343019 splice region variant G/A snp 0.46 0.41 0.010 1.000 1 2013 2013
dbSNP: rs2349775
rs2349775
5 0.846 0.107 7 8678450 intron variant G/A,C snp 0.80 0.010 < 0.001 1 2014 2014
dbSNP: rs2463107
rs2463107
2 1.000 0.036 12 79699537 intron variant A/C snp 0.34 0.010 1.000 1 2010 2010
dbSNP: rs2478813
rs2478813
4 0.878 0.071 1 208073865 intron variant A/G snp 0.85 0.010 1.000 1 2007 2007
dbSNP: rs2527367
rs2527367
4 0.878 0.071 7 74684804 5 prime UTR variant C/T snp 0.60 0.010 1.000 1 2016 2016
dbSNP: rs2973050
rs2973050
2 1.000 0.036 5 37817242 intron variant A/G,T snp 0.64 0.010 1.000 1 2014 2014
dbSNP: rs301430
rs301430
7 0.846 0.071 9 4576680 synonymous variant T/C snp 0.36 0.39 0.010 1.000 1 2010 2010
dbSNP: rs3093662
rs3093662
TNF
7 0.821 0.179 6 31576412 intron variant A/G snp 5.9E-02 0.010 1.000 1 2016 2016
dbSNP: rs3096140
rs3096140
4 0.878 0.071 5 37832731 intron variant G/A snp 0.68 0.010 1.000 1 2014 2014
dbSNP: rs324420
rs324420
36 0.657 0.321 1 46405089 missense variant C/A snp 0.24 0.28 0.010 1.000 1 2015 2015