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: rs6265
rs6265
171 0.463 0.679 11 27658369 missense variant C/T snp 0.19 0.15 0.100 0.944 18 2008 2016
dbSNP: rs759834365
rs759834365
157 0.471 0.679 11 27658456 missense variant C/T snp 1.2E-05 0.100 0.941 17 2008 2016
dbSNP: rs6313
rs6313
50 0.590 0.500 13 46895805 synonymous variant G/A snp 0.41 0.39 0.040 1.000 4 2007 2008
dbSNP: rs25531
rs25531
39 0.626 0.321 17 30237328 intergenic variant T/C snp 0.030 0.667 3 2015 2016
dbSNP: rs6295
rs6295
32 0.667 0.179 5 63962738 intron variant C/G snp 0.49 0.030 1.000 3 2013 2016
dbSNP: rs1800795
rs1800795
58 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.020 1.000 2 2010 2016
dbSNP: rs4680
rs4680
155 0.484 0.821 22 19963748 missense variant G/A snp 0.46 0.45 0.020 1.000 2 2013 2016
dbSNP: rs662
rs662
71 0.561 0.607 7 95308134 missense variant T/C snp 0.38 0.41 0.020 0.500 2 2007 2010
dbSNP: rs10473984
rs10473984
1 5 76971301 intron variant G/T snp 0.11 0.010 1.000 1 2010 2010
dbSNP: rs110402
rs110402
9 0.821 0.107 17 45802681 intron variant G/A,C snp 0.47; 3.2E-05 0.010 1.000 1 2015 2015
dbSNP: rs11046205
rs11046205
1 12 21839392 intron variant G/A snp 0.20 0.010 1.000 1 2013 2013
dbSNP: rs11632098
rs11632098
1 15 60855305 intron variant T/C snp 0.88 0.010 1.000 1 2016 2016
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: rs12137927
rs12137927
1 1 7811169 intron variant T/C snp 0.21 0.010 1.000 1 2016 2016
dbSNP: rs1360780
rs1360780
16 0.769 0.107 6 35639794 intron variant T/A,C snp 0.69 0.010 1.000 1 2015 2015
dbSNP: rs165599
rs165599
18 0.715 0.250 22 19969258 3 prime UTR variant G/A snp 0.57 0.010 1.000 1 2010 2010
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: rs17689882
rs17689882
5 0.923 0.071 17 45829462 intron variant G/A snp 0.13 0.010 1.000 1 2013 2013
dbSNP: rs1800497
rs1800497
36 0.662 0.250 11 113400106 missense variant G/A snp 0.26 0.26 0.010 1.000 1 2007 2007
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 2016 2016
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: rs2228305
rs2228305
3 0.923 0.107 17 82084916 missense variant C/T snp 4.1E-02 4.1E-02 0.010 1.000 1 2011 2011
dbSNP: rs2229094
rs2229094
8 0.878 0.143 6 31572779 stop gained T/C snp 0.27 0.26 0.010 1.000 1 2015 2015
dbSNP: rs2230912
rs2230912
10 0.769 0.143 12 121184393 missense variant A/G snp 0.13 0.12 0.010 1.000 1 2009 2009
dbSNP: rs2234693
rs2234693
50 0.590 0.571 6 151842200 intron variant T/C snp 0.47 0.010 1.000 1 2013 2013